Human immunodeficiency virus neutralizing antibodies and methods of use thereof

ABSTRACT

The invention provides broadly neutralizing antibodies directed to epitopes of Human Immunodeficiency Virus, or HIV. The invention further provides compositions containing HIV antibodies used for prophylaxis, and methods for diagnosis and treatment of HIV infection.

CROSS-REFERENCE TO RELATED APPLICATIONS

This application is a Continuation of U.S. patent application Ser. No. 15/719,738, filed Sep. 29, 2017, issued as U.S. Pat. No. 10,889,633, on Jan. 12, 2021, which is a Divisional of U.S. patent application Ser. No. 14/118,496, filed Jul. 25, 2014, issued as U.S. Pat. No. 9,783,594 on Oct. 10, 2017, which is a U.S. National Phase of International Application No. PCT/US2012/038400, filed May 17, 2012, which claims priority under 35 U.S.C. § 119(e) to U.S. Provisional Application No. 61/486,960, filed on May 17, 2011. The disclosures of which are hereby incorporated in their entirety.

STATEMENT REGARDING FEDERALLY FUNDED RESEARCH

The research leading to the present invention was supported in part, by National Institutes of Health Grant No. P01 A108677-01. Accordingly, the U.S. Government has certain rights in this invention.

FIELD OF THE INVENTION

The present invention relates to antibodies directed to epitopes of Human Immunodeficiency Virus (“HIV”). The present invention further relates to the preparation and use of broadly neutralizing antibodies directed to the HIV gp120 envelope protein for the prevention and treatment of HIV infection.

BACKGROUND OF THE INVENTION

HIV causes Acquired Immunodeficiency Syndrome (“AIDS”). The immune response to HIV infection in long-term non-progressors suggests that specific viral immunity may limit infection and the symptoms of disease. Some HIV infected individuals show broadly neutralizing IgG antibodies in their serum; little is known regarding the specificity and activity of these antibodies, despite their potential importance in designing effective vaccines, and no single characteristic has of yet been correlated with protective immunity. In animal models, passive transfer of neutralizing antibodies can contribute to protection against virus challenge. Neutralizing antibody responses also can be developed in HIV-infected individuals but the detailed composition of the serologic response is yet to be fully uncovered.

A number of immunologic abnormalities have been described in AIDS. These include, but are not limited to, abnormalities in B-cell function, abnormal antibody response, defective monocyte cell function, impaired cytokine production, depressed natural killer and cytotoxic cell function, defective ability of lymphocytes to recognize and respond to soluble antigens, and the depletion of the T4 helper/inducer lymphocyte population.

The amino acid and RNA sequences encoding HIV env from a number of HIV strains are known (Modrow, S. et al., J. Virology 61(2): 570 (1987)). The HIV virion is covered by a membrane or envelope derived from the outer membrane of host cells. This membrane contains a population of envelope glycoproteins (gp 160) anchored in the membrane bilayer at their carboxyl terminal region. Each glycoprotein contains two segments: the N-terminal segment, and the C-terminal segment. The N-terminal segment, called gp120 by virtue of its relative molecular weight of about 120 kD, protrudes into the aqueous environment surrounding the virion. The C-terminal segment, called gp41, spans the membrane. The N-terminal gp120 and the C-terminal gp41 are covalently linked by a peptide bond that is particularly susceptible to proteolytic cleavage. See European Patent Application Publication No. 0 335 635 to McCune et al and the references cited therein, each incorporated herein by reference in its entirety.

Several approaches to an AIDS vaccine have been proposed, including, but not limited to, inactivated and attenuated virus vaccines, subunit vaccines from virus-infected cells, recombinantly produced viral antigens, vaccines based on synthetic peptides, anti-idiotypic vaccines, and viral carrier-based vaccines. An additional approach to HIV therapeutic and prophylactic treatment includes making highly potent, broadly neutralizing monoclonal antibodies. Multiple studies have reported cloning and making monoclonal antibodies by various techniques for targeting the CD4 binding site as well as other parts of the virion spike and for neutralizing HIV. Generally, these techniques involve self-fusion or phage display techniques. Typically, in making HIV neutralizing antibodies using phage display techniques, random combinations of heavy and light chains are combined and a random pair is selected. Studies have reported a limited number of monoclonal antibodies, such as, for example, the phage display antibody b12, that are broadly highly potent, and broadly neutralizing (meaning antibodies that can neutralize multiple strains of HIV in sera) against HIV. The monoclonal antibody b12 is a broadly neutralizing antibody which has been reported to prevent HIV infection in macaques. Another broadly neutralizing antibody includes 2G12, which, atypically, has a structure which has yet to be seen in any other antibody with three combining sites. VRC01 is recently discovered broadly neutralizing antibody that targets the CD4 binding site (CD4bs) on the HIV spike. VRC01 was isolated by purifying single B cells that bind to a soluble, biotin labeled, stabilized, and re-surfaced core fragment of HIV gp120 (X. Wu et al., Science 329, 856 (Aug. 13, 2010)). Although successful, the isolation was inefficient, producing only 3 closely related HIV-binding antibodies from 25 million peripheral blood mononuclear cells from one individual. Like other anti-HIV antibodies obtained by the single cell antigen capture method, VRC01-3 showed very high levels of somatic mutations that were essential for potency and breadth. This high frequency of mutation is a potential impediment to antibody cloning because the mutated sequences may no longer be complementary to the primers used for cloning.

Some studies have reported that certain patients develop antibodies to HIV that are broadly neutralizing. Studies have reported that antibodies can be protective against initial HIV infection in passive transfer experiments in non-human primates and can modulate viral load during infection. See, for example, Mascola, 2000; Shibata, 1999; Veazey, 2003; Parren, 2001; Mascola, 1999; Trkola, 2005; Wei, 2003; Frost, 2005; Burton, 2004; Mascola, 2007; Karlsson Hedestam, 2008; McMichael, 2006; Zolla-Pazner, 2004.

BRIEF SUMMARY OF THE INVENTION

The present invention, in one embodiment, provides broadly neutralizing antibodies against HIV. In one embodiment, the present invention provides an isolated HIV antibody comprising a heavy chain comprising the consensus amino acid sequence: QXXLXQSGGXVKKPGXSVXVSCXASGYXXFXXYXIHWXRQAPGXGXXWVGXIXPRX GXXXXAXXFQGRLSLTRDXXXXXXTXXXFMDLXGLRXDDTAVYFCARXXXXXXXXX XXXXXXXXXDX (SEQ ID NO:1) wherein X indicates any amino acid or no amino acid.

In another embodiment, the present invention provides an isolated HIV antibody comprising a light chain comprising the consensus amino sequence: EIXLTQSPXSLSXSXGEXXTISCXXXQXXXXXXXLXWYQQRXGXAPRLLIXXXSXXXX GVPXRFSGXXXGXXYXLXISXLXXDDXAXYFCXXYEXXXXXXX (SEQ ID NO:2) wherein X indicates any amino acid or no amino acid.

In another embodiment, the present invention provides an isolated HIV antibody comprising a heavy chain comprising a highly conserved consensus sequence and a light chain comprising a highly conserved consensus sequence. The present invention further provides a method of producing an isolated HIV antibody comprising a heavy chain comprising a highly conserved consensus sequence and a light chain comprising a highly conserved consensus sequence.

In another embodiment, the present invention provides an isolated HIV antibody comprising the heavy chain consensus sequence of SEQ ID NO:1 and the light chain sequence of SEQ ID NO:2. In a further embodiment, the present invention provides an isolated HIV antibody comprising one or both of the heavy chain consensus sequence of SEQ ID NO:1 and the light chain sequence of SEQ ID NO:2, or sequences having at least 70%, or at least 80%, or at least 85%, or at least 90%, or at least 95%, or at least 97%, or at least 98%, or at least 99% identity thereto, with the proviso that the antibody does not have the amino acid sequence of VRC01.

In another embodiment, the present invention provides an isolated HIV antibody comprising one or both of the heavy chain consensus sequence of SEQ ID NO:1 and the light chain consensus sequence of SEQ ID NO:2 and wherein the antibody neutralizes HIV virus ZM53M.PB12 at an IC₅₀ concentration of less than 1.0 μg/ml, or HIV virus R1166.c1 at an IC₅₀ concentration of less than 1.0 μg/ml, or DU172.17 at an IC₅₀ concentration of less than 30 μg/ml. In another embodiment, the present invention provides an isolated HIV antibody comprising one or both of the heavy chain consensus sequence of SEQ ID NO:1 and the light chain consensus sequence of SEQ ID NO:2, wherein the antibody neutralizes a VRC01-resistant HIV virus at an IC₅₀ concentration of less than 30 μg/ml.

In another embodiment, the present invention provides an isolated HIV antibody selected from the group consisting of 3BNC117, 3BNC60, 12A12, 12A21, NIH45-46, 8ANC131, 8ANC134, IB2530, INC9 and 8ANC196.

In another embodiment, the present invention provides an isolated HIV antibody comprising heavy chain CDR1, CDR2 and CDR3 regions and light chain CDR1, CDR2 and CDR3 regions comprising the amino acid sequences of the corresponding regions of an HIV antibody selected from the group consisting of 3BNC117, 3BNC60, 12A12, 12A21, NIH45-46, bANC131, 8ANC134, IB2530, INC9 and 8ANC196.

In another embodiment, the present invention provides an isolated HIV antibody comprising a heavy chain comprising an amino acid sequence selected from the group consisting of SEQ ID NOs: 5-438.

In another embodiment, the present invention provides an isolated HIV antibody comprising a light chain comprising an amino acid sequence selected from the group consisting of SEQ ID NOs: 439-583.

In another embodiment, the present invention provides an isolated HIV antibody comprising a heavy chain and a light chain comprising an amino acid sequence set forth in Table A or Table B.

In another embodiment, the present invention provides an isolated HIV antibody comprising an insertion sequence comprising the amino acid sequence: ASWDFDF (SEQ ID NO:3).

In another embodiment, the present invention provides an isolated HIV antibody comprising an insertion sequence comprising the amino acid sequence: TARDY (SEQ ID NO:4).

In another embodiment, the present invention provides an isolated HIV antibody comprising insertion sequences SEQ ID No: 3 and SEQ ID No: 4.

In another embodiment, the present invention provides a method to improve the HIV neutralization potency and breadth of an isolated HIV antibody comprising inserting at least one of insertion sequences SEQ ID No: 3 and SEQ ID No: 4.

According to another embodiment, the present invention provides compositions comprising an isolated HIV antibody of the invention.

According to another embodiment, the present invention provides pharmaceutical compositions comprising an antibody of the invention and a pharmaceutically acceptable carrier.

According to another embodiment, the present invention provides nucleic acid molecules encoding an isolated HIV antibody of the invention.

According to other embodiments, the present invention provides vectors comprising nucleic acid molecules encoding an isolated HIV antibody of the invention, and cells comprising such vectors.

According to another embodiment, the present invention provides a method of preventing or treating HIV infection or an HIV-related disease comprising the steps of: identifying a mammalian subject in need of such prevention or treatment, and administering to said subject a therapeutically effective amount of at least one HIV antibody of the invention.

According to another embodiment, the method further comprises the administration of a second therapeutic agent. According to another embodiment, the second therapeutic agent is an antiviral agent.

Another embodiment of the present invention provides a method of reducing virus replication or spread of infection to additional host cells or tissues comprising contacting a mammalian cell with at least one antibody of the invention. According to another aspect, the present invention provides for a method for treating a mammalian subject infected with HIV, the method comprising administering to said subject a pharmaceutical composition comprising at least one antibody according to the invention.

According to another embodiment, the present invention provides a method for the preparation and administration of an HIV antibody preparation which is suitable for administration to a mammalian subject having or at risk of HIV infection, in an amount and according to a schedule sufficient to induce a protective immune response against HIV or reduction of the HIV virus in a mammalian subject. In another embodiment, the present invention provides a method for detecting an HIV antibody comprising a heavy chain comprising a highly conserved consensus sequence and a light chain comprising a highly conserved consensus sequence in a biological sample.

In another embodiment, the present invention provides the isolated antibodies of the invention for use in the treatment of HIV.

In another embodiment, the present invention provides a kit comprising a pharmaceutically acceptable dose unit of a pharmaceutically effective amount of at isolated HIV antibody of the invention, and a pharmaceutically acceptable dose unit of a pharmaceutically effective amount of an HIV agent selected from the group consisting of a non-nucleoside reverse transcriptase inhibitor, a protease inhibitor, a entry or fusion inhibitor and an integrase inhibitors, wherein the two pharmaceutically acceptable dose units can optionally take the form of a single pharmaceutically acceptable dose unit.

In another embodiment, the present invention provides a kit for the diagnosis, prognosis or monitoring the treatment of HIV in a subject comprising one or more detection reagents which specifically bind to anti-HIV neutralizing antibodies in a biological sample from a subject. In another aspect of the invention, the kit further provides reagents for performing PCR or mass spectrometry.

BRIEF DESCRIPTION OF THE DRAWINGS

FIGS. 1A, 1B, 1C and 1D show the HIV antibody neutralizing activity IC₅₀. (A) Limited panel. Top line indicates the donor number, then clone or antibody (Table 4); viruses are shown on the left. Colors indicate concentration at IC₅₀: red 0.1 μg/ml; orange 0.1-1 μg/ml; yellow 1-10 μg/ml; green 10 μg/ml; white not neutralized at any concentration tested. (B) Extended panel. (C) Neutralization summary graph comparing VRC01, NIH45-46, 3BNC117. Length of lines and size of circles inversely proportional to IC₅₀. Colors indicate viral clades: red A; blue B; green C; fucia D; black AE; gold AG. (D) Sequence of 3BNC60 (SEQ ID NO: 893), 1B2530 and 8ANC134 heavy chains with coverage by peptides found by Mass Spec in light grey. Red dots indicate differences from respective germline sequences.

FIGS. 2A, 2B and 2C show the binding properties of the HIV antibodies. (A) Representive SPR sensorgrams for binding to YU2-gp140 and 2CC-core by 12A12, 12A21 and 12A-germline (GL) reverted antibodies. (B) Graph shows K_(A) for representative antibodies. (C) Graph shows mean fluorescence intensity of anti-CD4i antibody binding to Bal.26 expressing 293T cells after incubation with the indicated antibodies. Table indicates whether or not an antibody induces CD4i site accessibility.

FIGS. 3A and 3B show the HIV antibody consensus sequence, and HIV antibody amino acid sequences. (A) Amino acid alignment relative to framework (FR) and CDR regions for consensus, germline genes, 10 selected antibodies and 8ANC195 (SEQ ID NOS 1 and 890-902, respectively, in order of appearance). Residues are numbered according to the 3BNC60 structure. (B) As in (A) for light chains (SEQ ID NOS 2 and 903-916, respectively, in order of appearance). (C, D, and E) Crystal structure of 3BNC60 Fab.

FIGS. 4A and 4B show recovery of highly mutated immunoglobulin heavy chains with specific primers. (A) side by side comparison of new and old primer set. Red boxes indicate successful amplification of IgV_(H) genes. FIG. 4A discloses SEQ ID NOS 917-979, respectively, in order of appearance). (B) HIV antibodies that bind to 2CC-core from Pt 8. Clonal families are shown by differently expanded slices. Two highly mutated clones that were not amplified with the old primer set are shown in striped pie slices.

FIGS. 5A and 5B show Ig V heavy (A) (SEQ ID NOS 980-984, respectively, in order of appearance) and light chain (B) (SEQ ID NOS 985-989, respectively, in order of appearance) sequences of new VRC01 clonal members.

FIGS. 6A and 6B show patient serum neutralizing activity. (A) Table summarizes purified serum IgG neutralizing activity against a panel of Tier 2 viruses in a Tzm-bl assay. Dark red boxes indicate IC₅₀ values below 10 μg/ml, orange between 10 and 100 μg/ml and yellow above 100 μg/ml. (B) dot plot summarizes the IC₅₀ values shown in A for the 4 more extensively tested patients.

FIGS. 7A and 7B demonstrate detection of antibodies by mass spectrometry. Collision activated dissociation MS/MS spectrum recorded on the doubly charged peptides HSDYCDFDVWGSGSQVIVSSASTK (SEQ ID NO: 888) from 3BNC153HC (A) and DGLGEVAPAYLYGIDAWGQGTTVIVTSASTK (SEQ ID NO: 889) from 8ANC134HC. (B. Observed b-type fragment ions (containing the N-terminus) and y-type fragment ions (containing the C-terminus) are labeled in the spectrum. Loss of water from fragment ions is indicated by *. Ions corresponding to the loss of water from the parent ion are labeled in the spectrum. Observed backbone cleavages are indicated in the sequence with ┐ for b-type ions and └ for y type ions.

FIGS. 8A and B demonstrate affinity of HIV antibodies. (A) Antibody binding to gp140 and 2CC-core measured by surface plasmon resonance (SPR). The SPR sensorgrams for antibody binding of the selected 3BNC-antibody clones are shown over time. (B) Bar graphs show the binding affinity (K_(A)) for gp140 and 2CC-core antigens for the selected IgG antibodies shown in A. RU, response units.

FIGS. 9A, 9B and 9C illustrate the somatic hypermutation analysis of selected HIV antibodies for (A) immunoglobulin heavy chain gene, (B) light chain kappa and (C) light chain lambda gene sequences. Sequences are aligned with their respective germline nucleotide sequences. Somatic mutations are shown in red letters, additionally gray boxes designate replacement mutations. Germline amino acid sequences with

indicating consensus residues are shown above the nucleotide alignment. FIG. 9A discloses SEQ ID NOS 991, 990, and 992-997; FIG. 9A Cont'd discloses SEQ ID NOS 999, 998, and 1000-1003; FIG. 9B discloses SEQ ID NOS 1005, 1004, and 1006-1009; FIG. 9B Cont'd discloses SEQ ID NOS 1011, 1010, and 1012-1015; and FIG. 9C discloses SEQ ID NOS 1017, 1016, and 1018-1019, all respectively, in order of appearance.

FIGS. 10A, 10B and 10C show antibody sequences from one expanded neutralizing clone in each (A) Patient (Pt)1, (B) Pt3 and (C) Pt8. Peptides identified by mass spectrometry are indicated in color. The variants marked with an asterisk are uniquely defined by one or more mass spectrometrically observed peptides (shown in light grey). The remaining mass spectrometrically observed peptides map non-uniquely to multiple variants as shown in dark grey. Underlined amino acids indicate non-tryptic cleavage sites in the variants shown. The cleavages are presumed to occur through chymotryptic cleavage or additional mutations (not observed among the cloned variants) that place a lysine or arginine residue at these sites. FIG. 10A discloses SEQ ID NOS 1020-1061; FIG. 10B discloses SEQ ID NOS 1062-1113; and FIG. 10C discloses SEQ ID NOS 1114-1138, all respectively, in order of appearance.

DETAILED DESCRIPTION OF THE INVENTION

I. HIV Neutralizing Antibodies

The present invention, in one embodiment, provides broadly neutralizing antibodies against HIV. In one embodiment, the present invention provides an isolated HIV antibody comprising a heavy chain comprising the consensus amino acid sequence: QXXLXQSGGXVKKPGXSVXVSCXASGYXXFXXYXIHWXRQAPGXGXXWVGXIXPRX GXXXXAXXFQGRLSLTRDXXXXXXTXXXFMDLXGLRXDDTAVYFCARXXXXXXXXX XXXXXXXXXDX (SEQ ID NO:1) wherein X indicates any amino acid or no amino acid.

In another embodiment, the present invention provides an isolated HIV antibody comprising a light chain comprising the consensus amino sequence: EIXLTQSPXSLSXSXGEXXTISCXXXQXXXXXXXLXWYQQRXGXAPRLLIXXXSXXXX GVPXRFSGXXXGXXYXLXISXLXXDDXAXYFCXXYEXXXXXXX (SEQ ID NO:2) wherein X indicates any amino acid or no amino acid.

In another embodiment, the present invention provides an isolated HIV antibody comprising the heavy chain sequence of SEQ ID NO:1 and the light chain sequence of SEQ ID NO:2. In a further embodiment, the present invention provides an isolated HIV antibody comprising one or both of the heavy chain sequence of SEQ ID NO:1 and the light chain sequence of SEQ ID NO:2, or sequences having at least 70%, or at least 80%, or at least 85%, or at least 90%, or at least 95%, or at least 97%, or at least 98%, or at least 99% identity thereto, with the proviso that the antibody does not have the amino acid sequence of VRC01. Percentage identity is determined as disclosed hereinbelow.

The present invention provides, in other embodiments, an isolated HIV antibody comprising a heavy chain comprising an highly conserved heavy chain amino acid sequence and a light chain comprising a highly conserved light chain amino acid sequence. A highly conserved heavy chain amino acid sequence is defined herein as an amino acid sequence having at least 70%, or at least 80%, or at least 85%, or at least 90%, or at least 95%, or at least 97%, or at least 98%, or at least 99% identity with the sequence of SEQ ID NO:1. A highly conserved light chain amino acid sequence is defined herein as an amino acid sequence having at least 70%, or at least 80%, or at least 85%, or at least 90%, or at least 95%, or at least 97%, or at least 98%, or at least 99% identity with the sequence of SEQ ID NO:2. Percentage identity is determined as disclosed hereinbelow.

In another embodiment, present invention provides an isolated HIV antibody comprising a heavy chain comprising an highly conserved heavy chain amino acid sequence and a light chain comprising a highly conserved light chain amino acid sequence, with the proviso that the antibody does not have the sequence of VRC01.

In another embodiment, the present invention provides an isolated HIV antibody comprising one or both of the heavy chain sequence of SEQ ID NO:1 and the light chain sequence of SEQ ID NO:2 and wherein the antibody neutralizes HIV virus ZM53M.PB12 at an IC₅₀ concentration of less than 1.0 μg/ml, or HIV virus R1166.c1 at an IC₅₀ concentration of less than 1.0 μg/ml, or DU172.17 at an IC₅₀ concentration of less than 30 μg/ml. In another embodiment, the present invention provides an isolated HIV antibody comprising one or both of the heavy chain sequence of SEQ ID NO:1 and the light chain sequence of SEQ ID NO:2, wherein the antibody neutralizes a VRC01-resistant HIV virus at an IC₅₀ concentration of less than 30 μg/ml. A VRC01-resistant HIV virus is defined herein as an HIV virus that is resistant to neutralization by VRC01 at an IC₅₀ value of 50 μg/ml. VRC01-resistant HIV viruses include, for example, H086.8, DU172.17, 250-4, 278-50, and 620345.c1.

In another embodiment, the present invention provides an isolated HIV antibody selected from the group consisting of 3BNC117, 3BNC60, 12A12, 12A21, NIH45-46, bANC131, 8ANC134, D32530, INC9 and 8ANC196.

In another embodiment, the present invention provides an isolated HIV antibody comprising heavy chain CDR1, CDR2 and CDR3 regions and light chain CDR1, CDR2 and CDR3 regions comprising the amino acids sequences of the corresponding regions of an HIV antibody selected from the group consisting of 3BNC117, 3BNC60, 12A12, 12A21, NIH45-46, bANC131, 8ANC134, IB2530, INC9 and 8ANC196.

In another embodiment, the present invention provides an isolated HIV antibody comprising a heavy chain comprising an amino acid sequence selected from the group consisting of SEQ ID NOs: 5-438.

In another embodiment, the present invention provides an isolated HIV antibody comprising a light chain comprising an amino acid sequence selected from the group consisting of SEQ ID NOs: 439-583.

In another embodiment, the present invention provides an isolated HIV antibody comprising a heavy chain and a light chain comprising an amino acid sequence set forth in Table A or Table B.

In another embodiment, the present invention provides an isolated HIV antibody comprising an insertion sequence comprising the amino acid sequence: ASWDFDF (SEQ ID NO:3). In a further embodiment, the present invention provides an isolated HIV antibody wherein insertion sequence SEQ ID No: 3, which corresponds to the FR3 region of the heavy chain commencing at amino acid 74 of 3BNC117 and 3BNC60 as shown in FIG. 5A, is substituted for the corresponding region, as determined by sequence alignment, of an HIV antibody of the invention. For example, SEQ ID No: 3 may be inserted after the seventh amino acid of FR3 of the heavy chain.

In another embodiment, the present invention provides an isolated HIV antibody comprising an insertion sequence comprising the amino acid sequence: TARDY (SEQ ID NO:4). In a further embodiment, the present invention provides an isolated HIV antibody wherein insertion sequence SEQ ID No: 4, which corresponds to the CDR3 region of the heavy chain commencing at amino acid 103 of NIH45-46 as shown in FIG. 5A, is substituted for the corresponding region, as determined by sequence alignment, of an HIV antibody of the invention. For example, SEQ ID No: 4 may be inserted after the fourth amino acid of CDR3 of the heavy chain.

In another embodiment, the present invention provides an isolated HIV antibody wherein insertion sequence SEQ ID No: 3, which corresponds to the FR3 region of the heavy chain commencing at amino acid 74 of 3BNC117 and 3BNC60 as shown in FIG. 5A, is substituted for the corresponding region, as determined by sequence alignment, of an HIV antibody of the invention, and insertion sequence SEQ ID No: 4, which corresponds to the CDR3 region of the heavy chain commencing at amino acid 103 of NIH45-46 as shown in FIG. 5A, is substituted for the corresponding region, as determined by sequence alignment, of an HIV antibody of the invention. For example, SEQ ID No: 3 may be inserted after the seventh amino acid of FR3 of the heavy chain and SEQ ID No: 4 may be inserted after the fourth amino acid of CDR3 of the heavy chain.

In another embodiment, the present invention provides a therapeutic composition comprising: i) a recombinantly produced monoclonal anti-HIV antibody or a gp120-derived antigen-binding fragment thereof comprising the CDR1, CDR2, and CDR3 regions of SEQ ID NO: 896, which corresponds to the variable heavy chain of NIH45-46 and the CDR1, CDR2, and CDR3 regions of SEQ ID NO: 910, which corresponds to the variable light chain of NIH45-46; and ii) a pharmaceutically acceptable carrier.

In a further embodiment, the present invention provides a method to improve the HIV neutralization potency and breadth of an isolated HIV antibody comprising making an isolated HIV antibody wherein insertion sequence SEQ ID No: 3, which corresponds to the FR3 region of the heavy commencing at amino acid 74 of 3BNC117 and 3BNC60 as shown in FIG. 5A, is substituted for the corresponding region, as determined by sequence alignment, of an HIV antibody of the invention and/or the insertion sequence SEQ ID No: 4, which corresponds to the CDR3 region of the heavy chain commencing at amino acid 103 of NIH45-46 as shown in FIG. 5A, is substituted for the corresponding region, as determined by sequence alignment, of an HIV antibody of the invention. For example, SEQ ID No: 3 may be inserted after the seventh amino acid of FR3 of the heavy chain, and/or SEQ ID No: 4 may be inserted after the fourth amino acid of CDR3 of the heavy chain. One skilled in this art can modify the amino acid sequence of an antibody utilizing recombinant methods and/or synthetic chemistry techniques for the production of a polypeptide or an antibody. Also, one skilled in the art can identify an improved HIV antibody with greater neutralization potency and breadth by using a HIV neutralization assay, as described below.

In another embodiment, the present invention provides an improved isolated HIV antibody comprising at least one of insertion sequences SEQ ID NO: 3 and SEQ ID NO: 4, wherein the improved isolated HIV antibody has greater HIV neutralization potency and breadth, than said isolated HIV antibody without insertion sequences SEQ ID NO: 3 and SEQ ID NO: 4. One skilled in the art can identify the improved HIV antibody with greater HIV neutralization potency and breadth by using the HIV neutralization assay, as described below.

One skilled in this art can modify the amino acid sequence of an antibody utilizing recombinant methods and/or synthetic chemistry techniques for the production of a polypeptide or an antibody.

In another embodiment, the present invention provides for a method to make an isolated HIV antibody comprising the heavy chain consensus sequence of SEQ ID NO:1 and the light chain sequence of SEQ ID NO:2. In a further embodiment, the present invention provides for a method of producing an isolated HIV antibody comprising one or both of the heavy chain consensus sequence of SEQ ID NO:1 and the light chain sequence of SEQ ID NO:2, or sequences having at least 70%, or at least 80%, or at least 85%, or at least 90%, or at least 95%, or at least 97%, or at least 98%, or at least 99% identity thereto, with the proviso that the antibody does not have the amino acid sequence of VRC01. Percentage identity is determined as disclosed hereinbelow.

In another embodiment, the present invention provides a method for detecting an isolated HIV antibody comprising obtaining an immunoglobulin-containing biological sample from a mammalian subject, isolating an HIV antibody from said sample, determining the amino sequence of the HIV antibody and identifying the presence of the heavy chain sequence of SEQ ID NO:1 and the light chain sequence of SEQ ID NO:2. In a further embodiment, the present invention provides for a method of selecting an isolated HIV antibody comprising determining the presence of one or both of the heavy chain consensus sequence of SEQ ID NO:1 and the light chain sequence of SEQ ID NO:2, or sequences having at least 70%, or at least 80%, or at least 85%, or at least 90%, or at least 95%, or at least 97%, or at least 98%, or at least 99% identity thereto, with the proviso that the antibody does not have the amino acid sequence of VRC01. Percentage identity is determined as disclosed herein below. The biological sample may be blood, serum, saliva, urine, sputum, a cell swab sample, or a tissue biopsy. The amino acid sequences may be determined by methods known in the art including, for example, PCR and mass spectrometry.

The term “antibody” (Ab) as used herein includes monoclonal antibodies, polyclonal antibodies, multispecific antibodies (for example, bispecific antibodies and polyreactive antibodies), and antibody fragments. Thus, the term “antibody” as used in any context within this specification is meant to include, but not be limited to, any specific binding member, immunoglobulin class and/or isotype (e.g., IgG1, IgG2, IgG3, IgG4, IgM, IgA, IgD, IgE and IgM); and biologically relevant fragment or specific binding member thereof, including but not limited to Fab, F(ab′)2, Fv, and scFv (single chain or related entity). It is understood in the art that an antibody is a glycoprotein comprising at least two heavy (H) chains and two light (L) chains inter-connected by disulfide bonds, or an antigen binding portion thereof. A heavy chain is comprised of a heavy chain variable region (VH) and a heavy chain constant region (CH1, CH2 and CH3). A light chain is comprised of a light chain variable region (VL) and a light chain constant region (CL). The variable regions of both the heavy and light chains comprise framework regions (FWR) and complementarity determining regions (CDR). The four FWR regions are relatively conserved while CDR regions (CDR1, CDR2 and CDR3) represent hypervariable regions and are arranged from NH2 terminus to the COOH terminus as follows: FWR1, CDR1, FWR2, CDR2, FWR3, CDR3, FWR4. The variable regions of the heavy and light chains contain a binding domain that interacts with an antigen while, depending of the isotype, the constant region(s) may mediate the binding of the immunoglobulin to host tissues or factors.

Also included in the definition of “antibody” as used herein are chimeric antibodies, humanized antibodies, and recombinant antibodies, human antibodies generated from a transgenic non-human animal, as well as antibodies selected from libraries using enrichment technologies available to the artisan.

The term “variable” refers to the fact that certain segments of the variable (V) domains differ extensively in sequence among antibodies. The V domain mediates antigen binding and defines specificity of a particular antibody for its particular antigen. However, the variability is not evenly distributed across the 110-amino acid span of the variable regions. Instead, the V regions consist of relatively invariant stretches called framework regions (FRs) of 15-30 amino acids separated by shorter regions of extreme variability called “hypervariable regions” that are each 9-12 amino acids long. The variable regions of native heavy and light chains each comprise four FRs, largely adopting a beta sheet configuration, connected by three hypervariable regions, which form loops connecting, and in some cases forming part of, the beta sheet structure. The hypervariable regions in each chain are held together in close proximity by the FRs and, with the hypervariable regions from the other chain, contribute to the formation of the antigen-binding site of antibodies (see, for example, Kabat et al., Sequences of Proteins of Immunological Interest, 5th Ed. Public Health Service, National Institutes of Health, Bethesda, Md. (1991)).

The term “hypervariable region” as used herein refers to the amino acid residues of an antibody that are responsible for antigen binding. The hypervariable region generally comprises amino acid residues from a “complementarity determining region” (“CDR”).

The term “monoclonal antibody” as used herein refers to an antibody obtained from a population of substantially homogeneous antibodies, i.e., the individual antibodies comprising the population are identical except for possible naturally occurring mutations that may be present in minor amounts. The term “polyclonal antibody” refers to preparations that include different antibodies directed against different determinants (“epitopes”).

The monoclonal antibodies herein include “chimeric” antibodies in which a portion of the heavy and/or light chain is identical with, or homologous to, corresponding sequences in antibodies derived from a particular species or belonging to a particular antibody class or subclass, while the remainder of the chain(s) is identical with, or homologous to, corresponding sequences in antibodies derived from another species or belonging to another antibody class or subclass, as well as fragments of such antibodies, so long as they exhibit the desired biological activity (see, for example, U.S. Pat. No. 4,816,567; and Morrison et al., Proc. Natl. Acad. Sci. USA, 81:6851-6855 (1984)). The described invention provides variable region antigen-binding sequences derived from human antibodies. Accordingly, chimeric antibodies of primary interest herein include antibodies having one or more human antigen binding sequences (for example, CDRs) and containing one or more sequences derived from a non-human antibody, for example, an FR or C region sequence. In addition, chimeric antibodies included herein are those comprising a human variable region antigen binding sequence of one antibody class or subclass and another sequence, for example, FR or C region sequence, derived from another antibody class or subclass.

A “humanized antibody” generally is considered to be a human antibody that has one or more amino acid residues introduced into it from a source that is non-human. These non-human amino acid residues often are referred to as “import” residues, which typically are taken from an “import” variable region. Humanization may be performed following the method of Winter and co-workers (see, for example, Jones et al., Nature, 321:522-525 (1986); Reichmann et al., Nature, 332:323-327 (1988); Verhoeyen et al., Science, 239:1534-1536 (1988)), by substituting import hypervariable region sequences for the corresponding sequences of a human antibody. Accordingly, such “humanized” antibodies are chimeric antibodies (see, for example, U.S. Pat. No. 4,816,567), wherein substantially less than an intact human variable region has been substituted by the corresponding sequence from a non-human species.

An “antibody fragment” comprises a portion of an intact antibody, such as the antigen binding or variable region of the intact antibody. Examples of antibody fragments include, but are not limited to, Fab, Fab′, F(ab′)2, and Fv fragments; diabodies; linear antibodies (see, for example, U.S. Pat. No. 5,641,870; Zapata et al., Protein Eng. 8(10): 1057-1062 [1995]); single-chain antibody molecules; and multispecific antibodies formed from antibody fragments.

“Fv” is the minimum antibody fragment that contains a complete antigen-recognition and antigen-binding site. This fragment contains a dimer of one heavy- and one light-chain variable region domain in tight, non-covalent association. From the folding of these two domains emanate six hypervariable loops (three loops each from the H and L chain) that contribute the amino acid residues for antigen binding and confer antigen binding specificity to the antibody. However, even a single variable region (or half of an Fv comprising only three CDRs specific for an antigen) has the ability to recognize and bind antigen, although at a lower affinity than the entire binding site.

“Single-chain Fv” (“sFv” or “scFv”) are antibody fragments that comprise the VH and VL antibody domains connected into a single polypeptide chain. The sFv polypeptide can further comprise a polypeptide linker between the VH and VL domains that enables the sFv to form the desired structure for antigen binding. For a review of sFv, see, for example, Pluckthun in The Pharmacology of Monoclonal Antibodies, vol. 113, Rosenburg and Moore eds., Springer-Verlag, New York, pp. 269-315 (1994); Borrebaeck 1995, infra.

The term “diabodies” refers to small antibody fragments prepared by constructing sFv fragments with short linkers (about 5-10 residues) between the VH and VL domains such that inter-chain but not intra-chain pairing of the V domains is achieved, resulting in a bivalent fragment, i.e., fragment having two antigen-binding sites. Bispecific diabodies are heterodimers of two “crossover” sFv fragments in which the VH and VL domains of the two antibodies are present on different polypeptide chains. Diabodies are described more fully in, for example, EP 404,097; WO 93/11161; and Hollinger et al., Proc. Natl. Acad. Sci. USA, 90:6444-6448 (1993).

Domain antibodies (dAbs), which can be produced in fully human form, are the smallest known antigen-binding fragments of antibodies, ranging from about 11 kDa to about 15 kDa. dAbs are the robust variable regions of the heavy and light chains of immunoglobulins (VH and VL, respectively). They are highly expressed in microbial cell culture, show favorable biophysical properties including, for example, but not limited to, solubility and temperature stability, and are well suited to selection and affinity maturation by in vitro selection systems such as, for example, phage display. dAbs are bioactive as monomers and, owing to their small size and inherent stability, can be formatted into larger molecules to create drugs with prolonged serum half-lives or other pharmacological activities. Examples of this technology have been described in, for example, WO9425591 for antibodies derived from Camelidae heavy chain Ig, as well in US20030130496 describing the isolation of single domain fully human antibodies from phage libraries.

Fv and sFv are the only species with intact combining sites that are devoid of constant regions. Thus, they are suitable for reduced nonspecific binding during in vivo use. sFv fusion proteins can be constructed to yield fusion of an effector protein at either the amino or the carboxy terminus of an sFv. See, for example, Antibody Engineering, ed. Borrebaeck, supra. The antibody fragment also can be a “linear antibody”, for example, as described in U.S. Pat. No. 5,641,870 for example. Such linear antibody fragments can be monospecific or bispecific.

In certain embodiments, antibodies of the described invention are bispecific or multispecific. Bispecific antibodies are antibodies that have binding specificities for at least two different epitopes. Exemplary bispecific antibodies can bind to two different epitopes of a single antigen. Other such antibodies can combine a first antigen binding site with a binding site for a second antigen. Alternatively, an anti-HIV arm can be combined with an arm that binds to a triggering molecule on a leukocyte, such as a T-cell receptor molecule (for example, CD3), or Fc receptors for IgG (Fc gamma R), such as Fc gamma RI (CD64), Fc gamma RII (CD32) and Fc gamma RIII (CD16), so as to focus and localize cellular defense mechanisms to the infected cell. Bispecific antibodies also can be used to localize cytotoxic agents to infected cells. Bispecific antibodies can be prepared as full length antibodies or antibody fragments (for example, F(ab′)2 bispecific antibodies). For example, WO 96/16673 describes a bispecific anti-ErbB2/anti-Fc gamma RIII antibody and U.S. Pat. No. 5,837,234 discloses a bispecific anti-ErbB2/anti-Fc gamma RI antibody. For example, a bispecific anti-ErbB2/Fc alpha antibody is reported in WO98/02463; U.S. Pat. No. 5,821,337 teaches a bispecific anti-ErbB2/anti-CD3 antibody. See also, for example, Mouquet et al., Polyreactivity Increases The Apparent Affinity Of Anti-HIV Antibodies By Heteroligation. NATURE. 467, 591-5 (2010).

Methods for making bispecific antibodies are known in the art. Traditional production of full length bispecific antibodies is based on the co-expression of two immunoglobulin heavy chain-light chain pairs, where the two chains have different specificities (see, for example, Millstein et al., Nature, 305:537-539 (1983)). Similar procedures are disclosed in, for example, WO 93/08829, Traunecker et al., EMBO J., 10:3655-3659 (1991) and see also; Mouquet et al., Polyreactivity Increases The Apparent Affinity Of Anti-HIV Antibodies By Heteroligation. NATURE. 467, 591-5 (2010).

Alternatively, antibody variable regions with the desired binding specificities (antibody-antigen combining sites) are fused to immunoglobulin constant domain sequences. The fusion is with an Ig heavy chain constant domain, comprising at least part of the hinge, CH2, and CH3 regions. According to some embodiments, the first heavy-chain constant region (CH1) containing the site necessary for light chain bonding, is present in at least one of the fusions. DNAs encoding the immunoglobulin heavy chain fusions and, if desired, the immunoglobulin light chain, are inserted into separate expression vectors, and are co-transfected into a suitable host cell. This provides for greater flexibility in adjusting the mutual proportions of the three polypeptide fragments in embodiments when unequal ratios of the three polypeptide chains used in the construction provide the optimum yield of the desired bispecific antibody. It is, however, possible to insert the coding sequences for two or all three polypeptide chains into a single expression vector when the expression of at least two polypeptide chains in equal ratios results in high yields or when the ratios have no significant affect on the yield of the desired chain combination.

Techniques for generating bispecific antibodies from antibody fragments also have been described in the literature. For example, bispecific antibodies can be prepared using chemical linkage. For example, Brennan et al., Science, 229: 81 (1985) describe a procedure wherein intact antibodies are proteolytically cleaved to generate F(ab′)2 fragments. These fragments are reduced in the presence of the dithiol complexing agent, sodium arsenite, to stabilize vicinal dithiols and prevent intermolecular disulfide formation. The Fab′ fragments generated then are converted to thionitrobenzoate (TNB) derivatives. One of the Fab′-TNB derivatives then is reconverted to the Fab′-thiol by reduction with mercaptoethylamine and is mixed with an equimolar amount of the other Fab′-TNB derivative to form the bispecific antibody. The bispecific antibodies produced can be used as agents for the selective immobilization of enzymes.

Other modifications of the antibody are contemplated herein. For example, the antibody can be linked to one of a variety of nonproteinaceous polymers, for example, polyethylene glycol, polypropylene glycol, polyoxyalkylenes, or copolymers of polyethylene glycol and polypropylene glycol. The antibody also can be entrapped in microcapsules prepared, for example, by coacervation techniques or by interfacial polymerization (for example, hydroxymethylcellulose or gelatin-microcapsules and poly-(methylmethacylate)microcapsules, respectively), in colloidal drug delivery systems (for example, liposomes, albumin microspheres, microemulsions, nano-particles and nanocapsules), or in macroemulsions. Such techniques are disclosed in, for example, Remington's Pharmaceutical Sciences, 16th edition, Oslo, A., Ed., (1980).

Typically, the antibodies of the described invention are produced recombinantly, using vectors and methods available in the art. Human antibodies also can be generated by in vitro activated B cells (see, for example, U.S. Pat. Nos. 5,567,610 and 5,229,275). General methods in molecular genetics and genetic engineering useful in the present invention are described in the current editions of Molecular Cloning: A Laboratory Manual (Sambrook, et al., 1989, Cold Spring Harbor Laboratory Press), Gene Expression Technology (Methods in Enzymology, Vol. 185, edited by D. Goeddel, 1991. Academic Press, San Diego, Calif.), “Guide to Protein Purification” in Methods in Enzymology (M. P. Deutshcer, ed., (1990) Academic Press, Inc.); PCR Protocols: A Guide to Methods and Applications (Innis, et al. 1990. Academic Press, San Diego, Calif.), Culture of Animal Cells: A Manual of Basic Technique, 2nd Ed. (R. I. Freshney. 1987. Liss, Inc. New York, N.Y.), and Gene Transfer and Expression Protocols, pp. 109-128, ed. E. J. Murray, The Humana Press Inc., Clifton, N.J.). Reagents, cloning vectors, and kits for genetic manipulation are available from commercial vendors such as BioRad, Stratagene, Invitrogen, ClonTech and Sigma-Aldrich Co.

Human antibodies also can be produced in transgenic animals (for example, mice) that are capable of producing a full repertoire of human antibodies in the absence of endogenous immunoglobulin production. For example, it has been described that the homozygous deletion of the antibody heavy-chain joining region (JH) gene in chimeric and germ-line mutant mice results in complete inhibition of endogenous antibody production. Transfer of the human germ-line immunoglobulin gene array into such germ-line mutant mice results in the production of human antibodies upon antigen challenge. See, for example, Jakobovits et al., Proc. Natl. Acad. Sci. USA, 90:2551 (1993); Jakobovits et al., Nature, 362:255-258 (1993); Bruggemann et al., Year in Immuno., 7:33 (1993); U.S. Pat. Nos. 5,545,806, 5,569,825, 5,591,669 (all of GenPharm); U.S. Pat. No. 5,545,807; and WO 97/17852. Such animals can be genetically engineered to produce human antibodies comprising a polypeptide of the described invention.

Various techniques have been developed for the production of antibody fragments. Traditionally, these fragments were derived via proteolytic digestion of intact antibodies (see, for example, Morimoto et al., Journal of Biochemical and Biophysical Methods 24:107-117 (1992); and Brennan et al., Science, 229:81 (1985)). However, these fragments can now be produced directly by recombinant host cells. Fab, Fv and ScFv antibody fragments can all be expressed in and secreted from E. coli, thus allowing the facile production of large amounts of these fragments. Fab′-SH fragments can be directly recovered from E. coli and chemically coupled to form F(ab′)2 fragments (see, for example, Carter et al., Bio/Technology 10:163-167 (1992)). According to another approach, F(ab′)2 fragments can be isolated directly from recombinant host cell culture. Fab and F(ab′)2 fragment with increased in vivo half-life comprising a salvage receptor binding epitope residues are described in U.S. Pat. No. 5,869,046. Other techniques for the production of antibody fragments will be apparent to the skilled practitioner.

Other techniques that are known in the art for the selection of antibody fragments from libraries using enrichment technologies, including but not limited to phage display, ribosome display (Hanes and Pluckthun, 1997, Proc. Nat. Acad. Sci. 94: 4937-4942), bacterial display (Georgiou, et al., 1997, Nature Biotechnology 15: 29-34) and/or yeast display (Kieke, et al., 1997, Protein Engineering 10: 1303-1310) may be utilized as alternatives to previously discussed technologies to select single chain antibodies. Single-chain antibodies are selected from a library of single chain antibodies produced directly utilizing filamentous phage technology. Phage display technology is known in the art (e.g., see technology from Cambridge Antibody Technology (CAT)) as disclosed in U.S. Pat. Nos. 5,565,332; 5,733,743; 5,871,907; 5,872,215; 5,885,793; 5,962,255; 6,140,471; 6,225,447; 6,291,650; 6,492,160; 6,521,404; 6,544,731; 6,555,313; 6,582,915; 6,593,081, as well as other U.S. family members, or applications which rely on priority filing GB 9206318, filed 24 May 1992; see also Vaughn, et al. 1996, Nature Biotechnology 14: 309-314). Single chain antibodies may also be designed and constructed using available recombinant DNA technology, such as a DNA amplification method (e.g., PCR), or possibly by using a respective hybridoma cDNA as a template.

Variant antibodies also are included within the scope of the invention. Thus, variants of the sequences recited in the application also are included within the scope of the invention. Further variants of the antibody sequences having improved affinity can be obtained using methods known in the art and are included within the scope of the invention. For example, amino acid substitutions can be used to obtain antibodies with further improved affinity. Alternatively, codon optimization of the nucleotide sequence can be used to improve the efficiency of translation in expression systems for the production of the antibody.

Such variant antibody sequences will share 70% or more (i.e., 80%, 85%, 90%, 95%, 97%, 98%, 99% or greater) sequence identity with the sequences recited in the application. Such sequence identity is calculated with regard to the full length of the reference sequence (i.e., the sequence recited in the application). Percentage identity, as referred to herein, is as determined using BLAST version 2.1.3 using the default parameters specified by the NCBI (the National Center for Biotechnology Information; http://www.ncbi.nlm.nih.gov/) [Blosum 62 matrix; gap open penalty=11 and gap extension penalty=1]. For example, peptide sequences are provided by this invention that comprise at least about 5, 10, 15, 20, 30, 40, 50, 75, 100, 150, or more contiguous peptides of one or more of the sequences disclosed herein as well as all intermediate lengths there between. As used herein, the term “intermediate lengths” is meant to describe any length between the quoted values, such as 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, etc.; 21, 22, 23, etc.; 30, 31, 32, etc.; 50, 51, 52, 53, etc.; 100, 101, 102, 103, etc.; 150, 151, 152, 153, etc.

The present invention provides for antibodies, either alone or in combination with other antibodies, such as, but not limited to, VRC01 and PG9, that have broad neutralizing activity in serum.

According to another embodiment, the present invention provides methods for the preparation and administration of an HIV antibody composition that is suitable for administration to a human or non-human primate patient having HIV infection, or at risk of HIV infection, in an amount and according to a schedule sufficient to induce a protective immune response against HIV, or reduction of the HIV virus, in a human.

According to another embodiment, the present invention provides a vaccine comprising at least one antibody of the invention and a pharmaceutically acceptable carrier. According to one embodiment, the vaccine is a vaccine comprising at least one antibody described herein and a pharmaceutically acceptable carrier. The vaccine can include a plurality of the antibodies having the characteristics described herein in any combination and can further include antibodies neutralizing to HIV as are known in the art.

It is to be understood that compositions can be a single or a combination of antibodies disclosed herein, which can be the same or different, in order to prophylactically or therapeutically treat the progression of various subtypes of HIV infection after vaccination. Such combinations can be selected according to the desired immunity. When an antibody is administered to an animal or a human, it can be combined with one or more pharmaceutically acceptable carriers, excipients or adjuvants as are known to one of ordinary skilled in the art. The composition can further include broadly neutralizing antibodies known in the art, including but not limited to, VRC01, PG9 and b12.

Further, with respect to determining the effective level in a patient for treatment of HIV, in particular, suitable animal models are available and have been widely implemented for evaluating the in vivo efficacy against HIV of various gene therapy protocols (Sarver et al. (1993b), supra). These models include mice, monkeys and cats. Even though these animals are not naturally susceptible to HIV disease, chimeric mice models (for example, SCID, bg/nu/xid, NOD/SCID, SCID-hu, immunocompetent SCID-hu, bone marrow-ablated BALB/c) reconstituted with human peripheral blood mononuclear cells (PBMCs), lymph nodes, fetal liver/thymus or other tissues can be infected with lentiviral vector or HIV, and employed as models for HIV pathogenesis. Similarly, the simian immune deficiency virus (SIV)/monkey model can be employed, as can the feline immune deficiency virus (FIV)/cat model. The pharmaceutical composition can contain other pharmaceuticals, in conjunction with a vector according to the invention, when used to therapeutically treat AIDS. These other pharmaceuticals can be used in their traditional fashion (i.e., as antiviral agents to treat HIV infection). Examples of HIV agents include without limitation non-nucleoside reverse transcriptase inhibitors, protease inhibitors, entry or fusion inhibitors and integrase inhibitors

According to another embodiment, the present invention provides an antibody-based pharmaceutical composition comprising an effective amount of an isolated HIV antibody, or an affinity matured version, which provides a prophylactic or therapeutic treatment choice to reduce infection of the HIV virus. The antibody-based pharmaceutical composition of the present invention may be formulated by any number of strategies known in the art (e.g., see McGoff and Scher, 2000, Solution Formulation of Proteins/Peptides: In McNally, E. J., ed. Protein Formulation and Delivery. New York, N.Y.: Marcel Dekker; pp. 139-158; Akers and Defilippis, 2000, Peptides and Proteins as Parenteral Solutions. In: Pharmaceutical Formulation Development of Peptides and Proteins. Philadelphia, Pa.: Talyor and Francis; pp. 145-177; Akers, et al., 2002, Pharm. Biotechnol. 14:47-127). A pharmaceutically acceptable composition suitable for patient administration will contain an effective amount of the antibody in a formulation which both retains biological activity while also promoting maximal stability during storage within an acceptable temperature range. The pharmaceutical compositions can also include, depending on the formulation desired, pharmaceutically acceptable diluents, pharmaceutically acceptable carriers and/or pharmaceutically acceptable excipients, or any such vehicle commonly used to formulate pharmaceutical compositions for animal or human administration. The diluent is selected so as not to affect the biological activity of the combination. Examples of such diluents are distilled water, physiological phosphate-buffered saline, Ringer's solutions, dextrose solution, and Hank's solution. The amount of an excipient that is useful in the pharmaceutical composition or formulation of this invention is an amount that serves to uniformly distribute the antibody throughout the composition so that it can be uniformly dispersed when it is to be delivered to a subject in need thereof. It may serve to dilute the antibody to a concentration which provides the desired beneficial palliative or curative results while at the same time minimizing any adverse side effects that might occur from too high a concentration. It may also have a preservative effect. Thus, for the antibody having a high physiological activity, more of the excipient will be employed. On the other hand, for any active ingredient(s) that exhibit a lower physiological activity, a lesser quantity of the excipient will be employed.

The above described antibodies and antibody compositions or vaccine compositions, comprising at least one or a combination of the antibodies described herein, can be administered for the prophylactic and therapeutic treatment of HIV viral infection.

The present invention also relates to isolated polypeptides comprising the amino acid sequences of the light chains and heavy chains listed in Tables A, B and FIGS. 10 A-C; the consensus sequences for the heavy and light chains of SEQ ID NOs: 1 and 2; and insertion sequences SEQ ID NOs:3 and 4.

In other related embodiments, the invention provides polypeptide variants that encode the amino acid sequences of the HIV antibodies listed in Tables A,B and FIG. 10 A-C; the consensus sequences for the heavy and light chains of SEQ ID NOs: 1 and 2; and insertion sequences SEQ ID NOs:3 and 4. These polypeptide variants have at least 70%, at least 75%, at least 80%, at least 85%, at least 90%, at least 95%, at least 96%, at least 97%, at least 98%, or at least 99%, or greater, sequence identity compared to a polypeptide sequence of this invention, as determined using the methods described herein, (for example, BLAST analysis using standard parameters). One skilled in this art will recognize that these values can be appropriately adjusted to determine corresponding identity of proteins encoded by taking into amino acid similarity and the like.

The term “polypeptide” is used in its conventional meaning, i.e., as a sequence of amino acids. The polypeptides are not limited to a specific length of the product. Peptides, oligopeptides, and proteins are included within the definition of polypeptide, and such terms can be used interchangeably herein unless specifically indicated otherwise. This term also includes post-expression modifications of the polypeptide, for example, glycosylations, acetylations, phosphorylations and the like, as well as other modifications known in the art, both naturally occurring and non-naturally occurring. A polypeptide can be an entire protein, or a subsequence thereof. Particular polypeptides of interest in the context of this invention are amino acid subsequences comprising CDRs, VH and VL, being capable of binding an antigen or HIV-infected cell.

A polypeptide “variant,” as the term is used herein, is a polypeptide that typically differs from a polypeptide specifically disclosed herein in one or more substitutions, deletions, additions and/or insertions. Such variants can be naturally occurring or can be synthetically generated, for example, by modifying one or more of the above polypeptide sequences of the invention and evaluating one or more biological activities of the polypeptide as described herein and/or using any of a number of techniques well known in the art.

For example, certain amino acids can be substituted for other amino acids in a protein structure without appreciable loss of its ability to bind other polypeptides (for example, antigens) or cells. Since it is the binding capacity and nature of a protein that defines that protein's biological functional activity, certain amino acid sequence substitutions can be made in a protein sequence, and, accordingly, its underlying DNA coding sequence, whereby a protein with like properties is obtained. It is thus contemplated that various changes can be made in the peptide sequences of the disclosed compositions, or corresponding DNA sequences that encode said peptides without appreciable loss of their biological utility or activity.

In many instances, a polypeptide variant will contain one or more conservative substitutions. A “conservative substitution” is one in which an amino acid is substituted for another amino acid that has similar properties, such that one skilled in the art of peptide chemistry would expect the secondary structure and hydropathic nature of the polypeptide to be substantially unchanged.

Amino acid substitutions generally are based on the relative similarity of the amino acid side-chain substituents, for example, their hydrophobicity, hydrophilicity, charge, size, and the like. Exemplary substitutions that take various of the foregoing characteristics into consideration are well known to those of skill in the art and include: arginine and lysine; glutamate and aspartate; serine and threonine; glutamine and asparagine; and valine, leucine and isoleucine.

“Homology” or “sequence identity” refers to the percentage of residues in the polynucleotide or polypeptide sequence variant that are identical to the non-variant sequence after aligning the sequences and introducing gaps, if necessary, to achieve the maximum percent homology. In particular embodiments, polynucleotide and polypeptide variants have at least about 70%, at least about 75%, at least about 80%, at least about 90%, at least about 95%, at least about 98%, or at least about 99% polynucleotide or polypeptide homology with a polynucleotide or polypeptide described herein.

Such variant polypeptide sequences will share 70% or more (i.e. 80%, 85%, 90%, 95%, 97%, 98%, 99% or more) sequence identity with the sequences recited in the application. In additional embodiments, the described invention provides polypeptide fragments comprising various lengths of contiguous stretches of amino acid sequences disclosed herein. For example, peptide sequences are provided by this invention that comprise at least about 5, 10, 15, 20, 30, 40, 50, 75, 100, 150, or more contiguous peptides of one or more of the sequences disclosed herein as well as all intermediate lengths there between.

The invention also includes nucleic acid sequences encoding part or all of the light and heavy chains of the described inventive antibodies, and fragments thereof. Due to redundancy of the genetic code, variants of these sequences will exist that encode the same amino acid sequences.

The present invention also includes isolated nucleic acid sequences encoding the polypeptides for the heavy and light chains of the HIV antibodies listed in Tables A, B and FIG. 10 A-C; the consensus sequences for the heavy and light chains of SEQ ID NOs: 1 and 2; and insertion sequences SEQ ID NOs:3 and 4.

In other related embodiments, the described invention provides polynucleotide variants that encode the peptide sequences of the heavy and light chains of the HIV antibodies listed in Tables A,B and FIGS. 10 A-C; the consensus sequences for the heavy and light chains of SEQ ID NOs: 1 and 2; and insertion sequences SEQ ID NOs:3 and 4. These polynucleotide variants have at least 70%, at least 75%, at least 80%, at least 85%, at least 90%, at least 95%, at least 96%, at least 97%, at least 98%, or at least 99%, or greater, sequence identity compared to a polynucleotide sequence of this invention, as determined using the methods described herein, (for example, BLAST analysis using standard parameters). One skilled in this art will recognize that these values can be appropriately adjusted to determine corresponding identity of proteins encoded by two nucleotide sequences by taking into account codon degeneracy, amino acid similarity, reading frame positioning, and the like.

The terms “nucleic acid” and “polynucleotide” are used interchangeably herein to refer to single-stranded or double-stranded RNA, DNA, or mixed polymers. Polynucleotides can include genomic sequences, extra-genomic and plasmid sequences, and smaller engineered gene segments that express, or can be adapted to express polypeptides.

An “isolated nucleic acid” is a nucleic acid that is substantially separated from other genome DNA sequences as well as proteins or complexes such as ribosomes and polymerases, which naturally accompany a native sequence. The term encompasses a nucleic acid sequence that has been removed from its naturally occurring environment, and includes recombinant or cloned DNA isolates and chemically synthesized analogues or analogues biologically synthesized by heterologous systems. A substantially pure nucleic acid includes isolated forms of the nucleic acid. Accordingly, this refers to the nucleic acid as originally isolated and does not exclude genes or sequences later added to the isolated nucleic acid by the hand of man.

A polynucleotide “variant,” as the term is used herein, is a polynucleotide that typically differs from a polynucleotide specifically disclosed herein in one or more substitutions, deletions, additions and/or insertions. Such variants can be naturally occurring or can be synthetically generated, for example, by modifying one or more of the polynucleotide sequences of the invention and evaluating one or more biological activities of the encoded polypeptide as described herein and/or using any of a number of techniques well known in the art.

Modifications can be made in the structure of the polynucleotides of the described invention and still obtain a functional molecule that encodes a variant or derivative polypeptide with desirable characteristics. When it is desired to alter the amino acid sequence of a polypeptide to create an equivalent, or even an improved, variant or portion of a polypeptide of the invention, one skilled in the art typically will change one or more of the codons of the encoding DNA sequence.

Typically, polynucleotide variants contain one or more substitutions, additions, deletions and/or insertions, such that the immunogenic binding properties of the polypeptide encoded by the variant polynucleotide is not substantially diminished relative to a polypeptide encoded by a polynucleotide sequence specifically set forth herein.

In additional embodiments, the described invention provides polynucleotide fragments comprising various lengths of contiguous stretches of sequence identical to or complementary to one or more of the sequences disclosed herein. For example, polynucleotides are provided by this invention that comprise at least about 10, 15, 20, 30, 40, 50, 75, 100, 150, 200, 300, 400, 500 or 1000 or more contiguous nucleotides of one or more of the sequences disclosed herein as well as all intermediate lengths there between and encompass any length between the quoted values, such as 16, 17, 18, 19, etc.; 21, 22, 23, etc.; 30, 31, 32, etc.; 50, 51, 52, 53, etc.; 100, 101, 102, 103, etc.; 150, 151, 152, 153, etc.; and including all integers through 200-500; 500-1,000.

In another embodiment of the invention, polynucleotide compositions are provided that are capable of hybridizing under moderate to high stringency conditions to a polynucleotide sequence provided herein, or a fragment thereof, or a complementary sequence thereof Hybridization techniques are well known in the art of molecular biology. For purposes of illustration, suitable moderate stringent conditions for testing the hybridization of a polynucleotide of this invention with other polynucleotides include prewashing in a solution of 5×SSC, 0.5% SDS, 1.0 mM EDTA (pH 8.0); hybridizing at 50-60° C., 5×SSC, overnight; followed by washing twice at 65° C. for 20 minutes with each of 2×, 0.5×, and 0.2×SSC containing 0.1% SDS. One skilled in the art will understand that the stringency of hybridization can be readily manipulated, such as by altering the salt content of the hybridization solution and/or the temperature at which the hybridization is performed. For example, in another embodiment, suitable highly stringent hybridization conditions include those described above, with the exception that the temperature of hybridization is increased, for example, to 60-65° C. or 65-70° C.

In some embodiments, the polypeptide encoded by the polynucleotide variant or fragment has the same binding specificity (i.e., specifically or preferentially binds to the same epitope or HIV strain) as the polypeptide encoded by the native polynucleotide. In some embodiments, the described polynucleotides, polynucleotide variants, fragments and hybridizing sequences, encode polypeptides that have a level of binding activity of at least about 50%, at least about 70%, and at least about 90% of that for a polypeptide sequence specifically set forth herein.

The polynucleotides of the described invention, or fragments thereof, regardless of the length of the coding sequence itself, can be combined with other DNA sequences, such as promoters, polyadenylation signals, additional restriction enzyme sites, multiple cloning sites, other coding segments, and the like, such that their overall length can vary considerably. A nucleic acid fragment of almost any length is employed. For example, illustrative polynucleotide segments with total lengths of about 10000, about 5000, about 3000, about 2000, about 1000, about 500, about 200, about 100, about 50 base pairs in length, and the like, (including all intermediate lengths) are included in many implementations of this invention.

In some embodiments, the polynucleotide sequences provided herein are used as probes or primers for nucleic acid hybridization, for example, as PCR primers. The ability of such nucleic acid probes to specifically hybridize to a sequence of interest enables them to detect the presence of complementary sequences in a given sample. However, other uses also are encompassed by the described invention, such as the use of the sequence information for the preparation of mutant species primers, or primers for use in preparing other genetic constructions. As such, nucleic acid segments of the described invention that include a sequence region of at least about a 15 nucleotide long contiguous sequence that has the same sequence as, or is complementary to, a 15 nucleotide long contiguous sequence disclosed herein is particularly useful. Longer contiguous identical or complementary sequences, for example, those of about 20, 30, 40, 50, 100, 200, 500, 1000 (including all intermediate lengths) including full length sequences, and all lengths in between, also are used in some embodiments.

Polynucleotide molecules having sequence regions consisting of contiguous nucleotide stretches of 10-14, 15-20, 30, 50, or even of 100-200 nucleotides or so (including intermediate lengths as well), identical or complementary to a polynucleotide sequence disclosed herein, are particularly contemplated as hybridization probes for use in, for example, Southern and Northern blotting, and/or primers for use in, for example, PCR. The total size of fragment, as well as the size of the complementary stretch(es), ultimately depends on the intended use or application of the particular nucleic acid segment. Smaller fragments generally are used in hybridization embodiments, wherein the length of the contiguous complementary region can be varied, such as between about 15 and about 100 nucleotides, but larger contiguous complementarity stretches can be used, according to the length complementary sequences one wishes to detect.

The use of a hybridization probe of about 15-25 nucleotides in length allows the formation of a duplex molecule that is both stable and selective. Molecules having contiguous complementary sequences over stretches greater than 12 bases in length can be utilized, though, in order to increase stability and selectivity of the hybrid, and thereby improve the quality and degree of specific hybrid molecules obtained. Nucleic acid molecules having gene-complementary stretches of 15 to 25 contiguous nucleotides, or even longer where desired, can be utilized.

Hybridization probes are selected from any portion of any of the sequences disclosed herein. All that is required is to review the sequences set forth herein, or to any continuous portion of the sequences, from about 15-25 nucleotides in length up to and including the full length sequence, that one wishes to utilize as a probe or primer. The choice of probe and primer sequences is governed by various factors. For example, one may wish to employ primers from towards the termini of the total sequence.

Further included within the scope of the invention are vectors such as expression vectors, comprising a nucleic acid sequence according to the invention. Cells transformed with such vectors also are included within the scope of the invention.

The present invention also provides vectors and host cells comprising a nucleic acid of the invention, as well as recombinant techniques for the production of a polypeptide of the invention. Vectors of the invention include those capable of replication in any type of cell or organism, including, for example, plasmids, phage, cosmids, and mini chromosomes. In some embodiments, vectors comprising a polynucleotide of the described invention are vectors suitable for propagation or replication of the polynucleotide, or vectors suitable for expressing a polypeptide of the described invention. Such vectors are known in the art and commercially available.

“Vector” includes shuttle and expression vectors. Typically, the plasmid construct also will include an origin of replication (for example, the ColE1 origin of replication) and a selectable marker (for example, ampicillin or tetracycline resistance), for replication and selection, respectively, of the plasmids in bacteria. An “expression vector” refers to a vector that contains the necessary control sequences or regulatory elements for expression of the antibodies including antibody fragment of the invention, in bacterial or eukaryotic cells.

As used herein, the term “cell” can be any cell, including, but not limited to, that of a eukaryotic, multicellular species (for example, as opposed to a unicellular yeast cell), such as, but not limited to, a mammalian cell or a human cell. A cell can be present as a single entity, or can be part of a larger collection of cells. Such a “larger collection of cells” can comprise, for example, a cell culture (either mixed or pure), a tissue (for example, endothelial, epithelial, mucosa or other tissue), an organ (for example, lung, liver, muscle and other organs), an organ system (for example, circulatory system, respiratory system, gastrointestinal system, urinary system, nervous system, integumentary system or other organ system), or an organism (e.g., a bird, mammal, or the like).

Polynucleotides of the invention may synthesized, whole or in parts that then are combined, and inserted into a vector using routine molecular and cell biology techniques, including, for example, subcloning the polynucleotide into a linearized vector using appropriate restriction sites and restriction enzymes. Polynucleotides of the described invention are amplified by polymerase chain reaction using oligonucleotide primers complementary to each strand of the polynucleotide. These primers also include restriction enzyme cleavage sites to facilitate subcloning into a vector. The replicable vector components generally include, but are not limited to, one or more of the following: a signal sequence, an origin of replication, and one or more marker or selectable genes.

In order to express a polypeptide of the invention, the nucleotide sequences encoding the polypeptide, or functional equivalents, may be inserted into an appropriate expression vector, i.e., a vector that contains the necessary elements for the transcription and translation of the inserted coding sequence. Methods well known to those skilled in the art may be used to construct expression vectors containing sequences encoding a polypeptide of interest and appropriate transcriptional and translational control elements. These methods include in vitro recombinant DNA techniques, synthetic techniques, and in vivo genetic recombination. Such techniques are described, for example, in Sambrook, J., et al. (1989) Molecular Cloning, A Laboratory Manual, Cold Spring Harbor Press, Plainview, N.Y., and Ausubel, F. M. et al. (1989) Current Protocols in Molecular Biology, John Wiley & Sons, New York. N.Y.

The present invention also provides kits useful in performing diagnostic and prognostic assays using the antibodies, polypeptides and nucleic acids of the present invention. Kits of the present invention include a suitable container comprising an HIV antibody, a polypeptide or a nucleic acid of the invention in either labeled or unlabeled form. In addition, when the antibody, polypeptide or nucleic acid is supplied in a labeled form suitable for an indirect binding assay, the kit further includes reagents for performing the appropriate indirect assay. For example, the kit may include one or more suitable containers including enzyme substrates or derivatizing agents, depending on the nature of the label. Control samples and/or instructions may also be included. The present invention also provide kits for detecting the presence of the HIV antibodies or the nucleotide sequence of the HIV antibody of the present invention in a biological sample by PCR or mass spectrometry.

“Label” as used herein refers to a detectable compound or composition that is conjugated directly or indirectly to the antibody so as to generate a “labeled” antibody. A label can also be conjugated to a polypeptide and/or a nucleic acid sequence disclosed herein. The label can be detectable by itself (for example, radioisotope labels or fluorescent labels) or, in the case of an enzymatic label, can catalyze chemical alteration of a substrate compound or composition that is detectable. Antibodies and polypeptides of the described invention also can be modified to include an epitope tag or label, for example, for use in purification or diagnostic applications. Suitable detection means include the use of labels such as, but not limited to, radionucleotides, enzymes, coenzymes, fluorescers, chemiluminescers, chromogens, enzyme substrates or co-factors, enzyme inhibitors, prosthetic group complexes, free radicals, particles, dyes, and the like.

According to another embodiment, the present invention provides diagnostic methods. Diagnostic methods generally involve contacting a biological sample obtained from a patient, such as, for example, blood, serum, saliva, urine, sputum, a cell swab sample, or a tissue biopsy, with an HIV antibody and determining whether the antibody preferentially binds to the sample as compared to a control sample or predetermined cut-off value, thereby indicating the presence of the HIV virus.

According to another embodiment, the present invention provides methods to detect the presence of the HIV antibodies of the present invention in a biological sample from a patient. Detection methods generally involve obtaining a biological sample from a patient, such as, for example, blood, serum, saliva, urine, sputum, a cell swab sample, or a tissue biopsy and isolating HIV antibodies or fragments thereof, or the nucleic acids that encode an HIV antibody, and assaying for the presence of an HIV antibody in the biological sample. Also, the present invention provides methods to detect the nucleotide sequence of an HIV antibody in a cell. The nucleotide sequence of an HIV antibody may also be detected using the primers disclosed herein. The presence of the HIV antibody in a biological sample from a patient may be determined utilizing known recombinant techniques and/or the use of a mass spectrometer.

In another embodiment, the present invention provides a method for detecting an HIV antibody comprising a heavy chain comprising a highly conserved consensus sequence and a light chain comprising a highly conserved consensus sequence in a biological sample, comprising obtaining an immunoglobulin-containing biological sample from a mammalian subject, isolating an HIV antibody from said sample, and identifying the highly conserved consensus sequences of the heavy chain and the light chain. The biological sample may be blood, serum, saliva, urine, sputum, a cell swab sample, or a tissue biopsy. The amino acid sequences may be determined by methods known in the art including, for example, PCR and mass spectrometry.

The term “assessing” includes any form of measurement, and includes determining if an element is present or not. The terms “determining”, “measuring”, “evaluating”, “assessing” and “assaying” are used interchangeably and include quantitative and qualitative determinations. Assessing may be relative or absolute. “Assessing the presence of” includes determining the amount of something present, and/or determining whether it is present or absent. As used herein, the terms “determining,” “measuring,” and “assessing,” and “assaying” are used interchangeably and include both quantitative and qualitative determinations.

II. Method of Reducing Viral Replication

Methods for reducing an increase in HIV virus titer, virus replication, virus proliferation or an amount of an HIV viral protein in a subject are further provided. According to another aspect, a method includes administering to the subject an amount of an HIV antibody effective to reduce an increase in HIV titer, virus replication or an amount of an HIV protein of one or more HIV strains or isolates in the subject.

According to another embodiment, the present invention provides a method of reducing viral replication or spread of HIV infection to additional host cells or tissues comprising contacting a mammalian cell with the antibody, or a portion thereof, which binds to an antigenic epitope on gp120.

III. Method of Treatment

According to another embodiment, the present invention provides a method for treating a mammal infected with a virus infection, such as, for example, HIV, comprising administering to said mammal a pharmaceutical composition comprising the HIV antibodies disclosed herein. According to one embodiment, the method for treating a mammal infected with HIV comprises administering to said mammal a pharmaceutical composition that comprises an antibody of the present invention, or a fragment thereof. The compositions of the invention can include more than one antibody having the characteristics disclosed (for example, a plurality or pool of antibodies). It also can include other HIV neutralizing antibodies as are known in the art, for example, but not limited to, VRC01, PG9 and b12.

Passive immunization has proven to be an effective and safe strategy for the prevention and treatment of viral diseases. (See, for example, Keller et al., Clin. Microbiol. Rev. 13:602-14 (2000); Casadevall, Nat. Biotechnol. 20:114 (2002); Shibata et al., Nat. Med. 5:204-10 (1999); and Igarashi et al., Nat. Med. 5:211-16 (1999), each of which are incorporated herein by reference). Passive immunization using human monoclonal antibodies provides an immediate treatment strategy for emergency prophylaxis and treatment of HIV.

Subjects at risk for HIV-related diseases or disorders include patients who have come into contact with an infected person or who have been exposed to HIV in some other way. Administration of a prophylactic agent can occur prior to the manifestation of symptoms characteristic of HIV-related disease or disorder, such that a disease or disorder is prevented or, alternatively, delayed in its progression.

For in vivo treatment of human and non-human patients, the patient is administered or provided a pharmaceutical formulation including an HIV antibody of the invention. When used for in vivo therapy, the antibodies of the invention are administered to the patient in therapeutically effective amounts (i.e., amounts that eliminate or reduce the patient's viral burden). The antibodies are administered to a human patient, in accord with known methods, such as intravenous administration, for example, as a bolus or by continuous infusion over a period of time, by intramuscular, intraperitoneal, intracerobrospinal, subcutaneous, intra-articular, intrasynovial, intrathecal, oral, topical, or inhalation routes. The antibodies can be administered parenterally, when possible, at the target cell site, or intravenously. In some embodiments, antibody is administered by intravenous or subcutaneous administration. Therapeutic compositions of the invention may be administered to a patient or subject systemically, parenterally, or locally. The above parameters for assessing successful treatment and improvement in the disease are readily measurable by routine procedures familiar to a physician.

For parenteral administration, the antibodies may formulated in a unit dosage injectable form (solution, suspension, emulsion) in association with a pharmaceutically acceptable, parenteral vehicle. Examples of such vehicles include, but are not limited, water, saline, Ringer's solution, dextrose solution, and 5% human serum albumin. Nonaqueous vehicles include, but are not limited to, fixed oils and ethyl oleate. Liposomes can be used as carriers. The vehicle may contain minor amounts of additives such as substances that enhance isotonicity and chemical stability, such as, for example, buffers and preservatives. The antibodies can be formulated in such vehicles at concentrations of about 1 mg/ml to 10 mg/ml.

The dose and dosage regimen depends upon a variety of factors readily determined by a physician, such as the nature of the infection, for example, its therapeutic index, the patient, and the patient's history. Generally, a therapeutically effective amount of an antibody is administered to a patient. In some embodiments, the amount of antibody administered is in the range of about 0.1 mg/kg to about 50 mg/kg of patient body weight. Depending on the type and severity of the infection, about 0.1 mg/kg to about 50 mg/kg body weight (for example, about 0.1-15 mg/kg/dose) of antibody is an initial candidate dosage for administration to the patient, whether, for example, by one or more separate administrations, or by continuous infusion. The progress of this therapy is readily monitored by conventional methods and assays and based on criteria known to the physician or other persons of skill in the art. The above parameters for assessing successful treatment and improvement in the disease are readily measurable by routine procedures familiar to a physician.

Other therapeutic regimens may be combined with the administration of the HIV antibody of the present invention. The combined administration includes co-administration, using separate formulations or a single pharmaceutical formulation, and consecutive administration in either order, wherein preferably there is a time period while both (or all) active agents simultaneously exert their biological activities. Such combined therapy can result in a synergistic therapeutic effect. The above parameters for assessing successful treatment and improvement in the disease are readily measurable by routine procedures familiar to a physician.

The terms “treating” or “treatment” or “alleviation” are used interchangeably and refer to both therapeutic treatment and prophylactic or preventative measures; wherein the object is to prevent or slow down (lessen) the targeted pathologic condition or disorder. Those in need of treatment include those already with the disorder as well as those prone to have the disorder or those in whom the disorder is to be prevented. A subject or mammal is successfully “treated” for an infection if, after receiving a therapeutic amount of an antibody according to the methods of the present invention, the patient shows observable and/or measurable reduction in or absence of one or more of the following: reduction in the number of infected cells or absence of the infected cells; reduction in the percent of total cells that are infected; and/or relief to some extent, one or more of the symptoms associated with the specific infection; reduced morbidity and mortality, and improvement in quality of life issues. The above parameters for assessing successful treatment and improvement in the disease are readily measurable by routine procedures familiar to a physician.

The term “therapeutically effective amount” refers to an amount of an antibody or a drug effective to treat a disease or disorder in a subject or mammal.

Administration “in combination with” one or more further therapeutic agents includes simultaneous (concurrent) and consecutive administration in any order.

“Carriers” as used herein include pharmaceutically acceptable carriers, excipients, or stabilizers that are nontoxic to the cell or mammal being exposed thereto at the dosages and concentrations employed. Often the physiologically acceptable carrier is an aqueous pH buffered solution. Examples of physiologically acceptable carriers include, but not limited to, buffers such as phosphate, citrate, and other organic acids; antioxidants including, but not limited to, ascorbic acid; low molecular weight (less than about 10 residues) polypeptide; proteins, such as, but not limited to, serum albumin, gelatin, or immunoglobulins; hydrophilic polymers such as, but not limited to, polyvinylpyrrolidone; amino acids such as, but not limited to, glycine, glutamine, asparagine, arginine or lysine; monosaccharides, disaccharides, and other carbohydrates including, but not limited to, glucose, mannose, or dextrins; chelating agents such as, but not limited to, EDTA; sugar alcohols such as, but not limited to, mannitol or sorbitol; salt-forming counterions such as, but not limited to, sodium; and/or nonionic surfactants such as, but not limited to, polyoxyethylenesorbitan monolaurate (e.g. TWEEN); polyethylene glycol (PEG), and poloxamers (e.g. PLURONICS).

Where a value of ranges is provided, it is understood that each intervening value, to the tenth of the unit of the lower limit unless the context clearly dictates otherwise, between the upper and lower limit of that range and any other stated or intervening value in that stated range is encompassed within the invention. The upper and lower limits of these smaller ranges which may independently be included in the smaller ranges is also encompassed within the invention, subject to any specifically excluded limit in the stated range. Where the stated range includes one or both of the limits, ranges excluding either both of those included limits are also included in the invention.

Unless defined otherwise, all technical and scientific terms used herein have the same meaning as commonly understood by one of ordinary skill in the art to which this invention belongs. Although any methods and materials similar or equivalent to those described herein can also be used in the practice or testing of the present invention, the preferred methods and materials are now described. All publications mentioned herein are incorporated herein by reference in their entireties.

As used herein and in the appended claims, the singular forms “a”, “and” and “the” include plural references unless the context clearly dictates otherwise

Publications disclosed herein are provided solely for their disclosure prior to the filing date of the present invention. Nothing herein is to be construed as an admission that the present invention is not entitled to antedate such publication by virtue of prior invention. Further, the dates of publication provided may be different from the actual publication dates which may need to be independently confirmed.

Each of the applications and patents cited in this text, as well as each document or reference, patient or non-patient literature, cited in each of the applications and patents (including during the prosecution of each issued patent; “application cited documents”), and each of the PCT and foreign applications or patents corresponding to and/or claiming priority from any of these applications and patents, and each of the documents cited or referenced in each of the application cited documents, are hereby expressly incorporated herein by reference in their entirety. More generally, documents or references are cited in this text, either in a Reference List before the claims; or in the text itself; and, each of these documents or references (“herein-cited references”), as well as each document or reference cited in each of the herein-cited references (including any manufacturer's specifications, instructions, etc.), is hereby expressly incorporated herein by reference.

The following non-limiting examples serve to further illustrate the present invention.

Example 1 Materials, Methods and Instrumentation

Samples. Human samples were collected after signed informed consent in accordance with Institutional Review Board (IRB)-reviewed protocols by all participating institutions. Patient 1 was selected from a cohort of long-term non-progressors followed at the Aaron Diamod Aids Research Center, New York. Patients 3 and 8 were selected from a group of elite controllers that were followed at the Ragon Institute in Boston. Patients 1, 3 and 8 were selected based on their broad neutralizing serum activity against a standard panel of HIV isolates. Patient 12 was selected from the Protocol G Cohort of the “International Aids Vaccine Initiative” based on broad serum neutralizing activity.

Staining, single-cell sorting and antibody cloning. Staining and single cell sorting of 2CC-Core and gp140 specific Ig+ memory B cells was performed (J. F. Scheid et al., Nature 458, 636 (Apr. 2, 2009)). Briefly, CD19+ B cells were enriched from peripheral blood mononuclear cells using anti human CD19 magnetic MACS beads (Miltenyi Biotec) and subsequently stained with anti human CD20 and anti human IgG antibodies (Becton Dickinson) as well as biotinylated 2CC-Core (B. Dey et al., PLoS Pathog 5, e1000445 (May, 2009)) or YU2-gp140 trimer (R. Diskin, P. M. Marcovecchio, P. J. Bjorkman, Nat Struct Mol Biol 17, 608 (May, 2010)) followed by detection with streptavidin coupled phycoerythrin (PE, Beckton Dickinson). Single cells were sorted on a FACSAria III cell sorter (Becton Dickinson), excluding cell doublets, into 96-well PCR plates (Denville) containing 4 μl/well of ice-cold 0.5× phosphate-buffered saline (PBS) containing 10 mM DTT, 8 U RNAsin® (Promega), 0.4 U 5′-3′ Prime RNAse Inhibitor™ (Eppendorf). Plates were sealed with Microseal® ‘F’ Film (BioRad), immediately frozen on dry ice before storage at −80° C.

cDNA synthesis and Ig amplification were performed (H. Wardemann et al., Science 301, 1374 (Sep. 5, 2003)) with following modifications:

Instead of using the original primer sets, first and second immunoglobulin specific PCRs were carried out using the primers described in Table 1 in a semi-nested approach. Cloning of heavy and light chain PCR products into their respective expression vectors was performed and 100% identity of cloned expression plasmids with the original PCR product confirmed by sequencing before expression of the antibodies in HEK 293 cells.

ELISAs. High-binding 96-well ELISA plates (Costar) were coated overnight with 100 ng/well of purified antigens (gp140, gp120, gp41, gp120^(core) and 2CC-core) (B. Dey et al., PLoS Pathog 5, e1000445 (May, 2009)) and mutant proteins (gp120 D368R, gp120 I420R) in PBS. After washing, plates were blocked 2 h with 2% BSA, 1 μM EDTA, 0.05% Tween-PBS (Blocking buffer) and then, incubated 2h with IgG antibodies diluted at 4 μg/ml and several consecutive 1:4 dilutions in PBS. After washing, the plates were developed by incubation for 1 h with goat HRP-conjugated anti-mouse IgG (Jackson ImmunoReseach) (at 0.8 μg/ml in blocking buffer) and by adding 100 μl of HRP chromogenic substrate (ABTS solution, Invitrogen). Optical densities were measured at 405 nm (OD_(405 nm)) using an ELISA microplate reader (Molecular Devices). Background values given by incubation of PBS alone in coated wells were subtracted. IgG Antibodies were tested for polyreactivity (H. Mouquet et al., Nature 467, 591 (Sep. 30, 2010)) and considered polyreactive when they recognized at least two structurally different antigens out of the four tested; ssDNA, dsDNA, insulin, and LPS. Threshold values for reactivity were determined by using control antibodies mGO53 (negative), eiJB40 (low positive), and ED38 (high positive).

Neutralization assays: Neutralization screens were performed (D. C. Montefiori, Curr Protoc Immunol Chapter 12, Unit 12 11 (January, 2005)). In brief, neutralization was detected as reduction in luciferase reporter gene expression after single round infection in Tzm-bl cells. In order to rule out unspecific antiviral activity in antibody samples MuLV (murine leukemia virus) was used as a negative control.

Clone specific identification of bone marrow plasma cells. Bone marrow plasma cells were stained with anti human CD138 and anti CD19 antibodies (Becton Dickinson) after Ficoll purification of mononuclear cells from bone marrow aspirates using Ficoll-Paque (GE Healthcare). CD138+CD19+ human plasma cells were bulk sorted on a FACSAriaIII cell sorter (Becton Dickinson) and RNA isolation performed on 100,000 cells using Trizol LS reagent (Invitrogen) according to the manufacturers instructions. RNA was reverse transcribed using Superscript III reverse transcriptase (Invitrogen) according to manufacturers instructions. cDNA was then subjected to Immunoglobulin specific PCR with following modifications: 1 μl of cDNA was amplified in 2 rounds of nested immunoglobulin heavy chain clone specific PCR using first round forward leader and constant region reverse primers shown in Table 1 followed by clone specific forward and reverse primers designed based on sequencing results from single cell analysis. PCR products were gel purified and cloned into TOPO TA vectors (Invitrogen) according to the manufacturers instructions. Colonies were screened by PCR with clone specific primers and sequenced.

Surface plasmon resonance. All experiments were performed with a Biacore T100 (Biacore, Inc) in HBS-EP+ running buffer (Biacore, Inc) at 25° C. as described previously (Mouquet2010). YU-2 gp140 and 2CC-core proteins at 12.5 μg/mL were immobilized on CMS chips (Biacore, Inc.) by amine coupling at pH 4.5 resulting in an immobilization level of 100 RUs. For kinetic measurements on the gp140- and 2CC-core-derivatized chips, IgGs were injected through flow cells at 700 nM and 4 successive 1:2-dilutions in HBS-EP+ running buffer (Biacore, Inc.) at flow rates of 40 μL/min with 3 min association and 5 min dissociation. The sensor surface was regenerated between each experiment with a 30 second injection of 10 mM glycine-HCl pH 2.5 at a flow rate of 50 μL/min. Off rate (k_(d) (s⁻¹)), on rate (k_(a) (M⁻¹s⁻¹) and binding constants (K_(D) (M) or K_(A) (M⁻¹) were calculated after subtraction of backgrounds (binding to control flow cells and signal of the HBS-EP+ running buffer) using Biacore T100 Evaluation software using the kinetic analysis and the 1:1 binding model. The sensorgrams showed in FIG. 2 and FIG. 8 are derived from the Biacore data processing using Scrubber 2 software (Center for Biomolecular Interaction Analysis, University of Utah).

CD4i site induction. 293T cells were transfected with gp160^(BAL.26)Δc or gp160^(YU.2)Δc in a pMX-IRES-GFP construct (Pietzsch et al. 2010) using Fugene™6 (Roche) at a 1:2 plasmid:Fugene ratio. After 48 hours 293T cells were washed with PBS and detached with Trypsin-free cell dissociation buffer (Gibco) and resuspended at a concentration of 10⁷ cells/ml in FACS buffer (1×PBS, 2% FBS, 2 mM EDTA). sCD4 (Progenics Pharmaceuticals, Inc.) and mAbs were added to gp160-expressing 293T cells in a 1:4 dilution series starting with a final concentration of 40 μg/ml. mGO is a negative control antibody that does not bind to gp160Ac (H. Mouquet et al., Nature 467, 591 (Sep. 30, 2010)). After incubation for 15 min on ice cells were split and stained for 25 min on ice with an Alexa647-labeled CD4-induced site mAb (3-67; (J. F. Scheid et al., Nature 458, 636 (Apr. 2, 2009)) or an Alexa647-labeled control mAb (i.e. PG16; L. M. Walker et al., Science 326, 285 (Oct. 9, 2009)) or 2G12 for gp160^(YU.2) and 2G12 for gp160^(BAL.26)). Antibody labeling was performed by using Alexa Fluor® 647 Microscale Protein Labeling Kit (Invitrogen). Cells were analyzed on an LSRFortessa cell analyzer (BD Bioscience).

Crystallization. The 3BNC60 IgG was expressed by transient expression in HEK293-6E cells and prepared the Fab fragment was prepared by papain cleavage (R. Diskin, P. M. Marcovecchio, P. J. Bjorkman, Nat Struct Mol Biol 17, 608 (May, 2010). Crystallization screens were conducted at 20° C. by vapor diffusion in nL sitting drops using a Mosquito™ (TTP LabTech) crystallization robot on MRC crystallization plates (Jena Bioscience). We combined 3BNC60 Fab at a concentration of 9.5 mg/ml with reservoir solution in a 1:1 ratio to create 400 nL drops. Initial crystallization hits were obtained using the PEGRx HT™ (Hampton Research) crystallization screen and further optimized manually. Crystals suitable for data collection grew after several weeks in 11.7% polyethylene glycol 20,000, 0.1 M sodium acetate pH 5.0, 100 mM potassium/sodium tartrate, 20 mM lithium sulfate, 10 mM N-Cyclohexyl-2-aminoethanesulfonic acid (CHES) pH 9.5 in the monoclinic space group P2₁ with two Fabs in the asymmetric unit. Crystals were soaked in reservoir solution supplemented with 15% glycerol for 2 hours before immersing in reservoir solution supplemented with 30% glycerol and flash cooling in liquid nitrogen. Diffraction data were collected at the Stanford Synchrotron Radiation Lightsource (SSRL) beam-line 12-2 at 100 K using a Pilatus 6M detector. Data were indexed, integrated, and scaled using XDS W. Kabsch, Acta Crystallogr D Biol Crystallogr 66, 125 (February, 2010) (Table 8). Molecular replacement was conducted using Phaser with the V_(H) and C_(H)1 domains from the anti-tumor antibody CTM01 (PDB code 1AD9) and with the V_(L) and C_(L) domains of the anti-gp120 b13 antibody (PDB code 3IDX) as search models. Model building and refinement to 2.65 Å resolution was done iteratively using Phenix P. Emsley, B. Lohkamp, W. G. Scott, K. Cowtan, Acta Crystallogr D Biol Crystallogr 66, 486 (April, 2010) and Coot (P. Emsley, B. Lohkamp, W. G. Scott, K. Cowtan, Acta Crystallogr D Biol Crystallogr 66, 486 (April, 2010)). The structure was refined using a maximum-likelihood target function and non-crystallographic symmetry restraints. The final model (R_(work)=20.7%; R_(free)=25.7%) includes 6478 protein atoms, 146 water molecules and 28 sugar atoms (Table 8). 91.9%, 7.6% and 0.5% of the residues were in the favored, allowed, and disallowed regions, respectively, of the Ramachandran plot. Structural analyses and visualization were done using PyMol (The PyMOL Molecular Graphics System, Version 1.3, Schrödinger, LLC). The 3BNC60 structure consists of residues 3-205 for the light chain (including the first N-acetylglucosamine within an N-linked carbohydrate attached to Asn72) and 2-217 for the heavy-chain. Residues at the termini residues and residues 133-140 within the C_(H)1 domain are disordered.

Mass Spectrometry. IgG was purified from serum using ProteinG Sepharose (GE Healthcare) according to the manufacturers instructions. IgGs were then digested with immobilized papain (Pierce) and digested Fab-Fc fragment mixes incubated with saturating quantities of biotinylated 2CC-Core protein. Streptavidin coupled Dynabeads (Invitrogen) were added after incubation for 15 minutes at room temperature and subjected to 10 rounds of washing with Phosphate Buffered Saline (Gibco). Bound Fab fragments were eluted with lithium dodecyl sulfate buffer (Invitrogen) at 95 C and sample purity confirmed with SDS-polyacrylamide gel electrophoresis followed by silver stain or coomassie staining before analysis by mass spectrometry.

Isolated Fab fragments were reduced with dithiothreitol, alkylated using iodoacetamide, resolved by 1D gel electrophoresis on a 4-12% NuPAGE Novex Bis-Tris gel (Invitrogen), and stained with Coomassie Blue (Thermo Fisher). The Fab fragments were excised from the gel, and digested using 200 ng of trypsin (Promega). The resulting peptides were isolated using reverse phase resin (PORS 20 R2, Applied Biosystem) and eluted using an aliquot of 40% acetonitrile in 0.5% acetic acid and a second aliquot of 80% acetonitrile in 0.5% acetic acid. Acetonitrile was removed using a speedvac (Thermo Fisher Scientific) and aliquots of the remaining solution pressure loaded onto self-packed PicoFrit® column (New Objective, Woburn, Mass.) with integrated emitter tip (360 μm O.D., 50 μm I.D., 10 μm tip), packed with 6 cm of reverse-phase C18 material (ReproSil-Pur C18-AQ, 3 μm beads from Dr. Maisch GmbH) and interfaced to a Agilent 1200 series HPLC system (Agilent) with either a LTQ Orbitrap™ XL mass spectrometer or a LTQ Orbitrap Velos™ mass spectrometer (Thermo Fisher Scientific) using a home-built micro electrospray source. The peptides were eluted into the mass spectrometer with the following gradient: 0 to 5% B in 5 min, 40% B in 125 min, 60% B in 150 min, 100% B in 165 min (A=0.1 M acetic acid, B=70% acetonitrile in 0.1 M acetic acid, flow rate 90 nL/min). Both instruments were operated in the data dependent mode and for both mass spectrometers the target value was set to 5e5 ions and a resolution of 60,000 (at 400 m/z). For analysis on the LTQ Orbitrap™ XL a full scan was followed by 8 MS/MS scans on the 8 most abundant ions from that full scan. The peptides (only charge states >1) were isolated with a 2 Da window, target window of 1e4 ions, dissociated via CAD (normalized collision energy=35, activation Q=0.25, activation time 30 msec) and mass analyzed in the LTQ. For analysis on the LTQ Orbitrap™ Velos a full scan was followed by 10 MS/MS scans at 7,500 resolution on the 10 most abundant ions from the immediate preceding full scan. The peptides (only charge state >2) were isolated with a 3 Da window, target window of 2e5 ions, dissociated via HCD (normalized collision energy=40, activation time 0.100 msec) and mass analyzed in the Orbitrap. For either instrument the ions selected for MS/MS were set on an exclusion list for 30 seconds. The resulting MS/MS spectra were searched against the Human IPI and in-house patient specific IgG database using Xtandem!, peptides were automatically compared to tryptic peptides in the human IPI and our in-house patient specific database. Peptide hits corresponding to patient specific IgG were manually confirmed.

Multiple sequence alignments. All multiple sequence alignments were conducted using CLUSTALW2 with default parameters (weight matrix: GONNET for proteins and UM for DNA, gap open=10, gap extension 0.1). Alignments shading were generated using TeXshade package.

Alignment consensus. The consensus sequences for multiple alignments were generated based on identity and similarity between residues (>=70%). The amino acids were grouping due similarity as: FYW, ILVM, RK, DE, GA, ST and NQ.

Phylogenetic Germline Trees. The relationship between sequences was generated using the Neighbor-Joining method. The bootstrap consensus tree inferred from 1000 replicates was taken to represent the relationship. Branches corresponding to partitions reproduced in less than 50% bootstrap replicates are collapsed. The percentage of replicate trees in which the associated sequence clustered together in the bootstrap test (1000 replicates) are shown next to the branches. The tree is drawn to scale, with branch lengths in the same units as those of the evolutionary distances used to infer the phylogenetic tree. The evolutionary distances were computed using the number of differences method and are in the units of the number of amino acid differences per sequence. All ambiguous positions were removed for each sequence pair. Evolutionary analyses were conducted in MEGA5.

R/S Ratio Calculation. DNA sequences were superposed over the proteins alignments to replacement/substitution calculation. All gaps positions were removed from the analysis. The R/S ratio analysis was conducted using Perl scripts.

Example 2 Isolating HIV Antibodies

To determine whether HIV antibody cloning is limited because of somatic mutation, a new series of primers was designed to avert this potential problem (Table 1). The new primer set was tested by sorting B cells that bind to an HIV-gp120 core protein lacking the V1-3 loops and containing a pair of stabilizing disulfide bonds (2CC-core). In contrast to the re-surfaced bait used to clone VRC01, the 2CC-core bait also allows capture of antibodies to the CD4-induced co-receptor binding site (CD4i).

In side-by-side comparisons, the new primer set increased recovery of IgH chains when compared to the initial primer set (FIG. 4(a)). The antibodies obtained with the new primer set were more mutated (average 35.6 vs. 19.8 p=<0.0001 and maximum 85 vs. 50 for IgH) and included clones that were not found with the original primer set (FIG. 4(a)). To determine whether the new primers rescue VRC01-like antibodies from cells that had been sorted with YU2 gp140, frozen cDNA samples from that individual which had already been examined exhaustively with the original primer set without producing any VRC01 related clones were examined. In 80 wells, 3 antibodies corresponding to VRC01 variants as determined by the IgH and IgL sequences were found (FIGS. 5A and B). It was concluded that VRC01-like antibodies were captured by the gp140 trimer, and that primers that were specifically designed to clone highly mutated antibodies captured a larger fraction of anti-HIV antibodies from the memory B cells of patients with high titers of broadly neutralizing antibodies.

Four unrelated HIV infected individuals, including 2 Caucasians, 1 Hispanic and 1 African donor, showing high titers of broadly neutralizing antibodies were examined using the 2CC-core bait, including 2 individuals whose previously cloned antibodies could not account for their serologic activity (Table 2 and FIGS. 6A and B). 576 antibodies representing 201 different unique and diversified clones were obtained from a starting population of 1.5×10⁵ IgG⁺ memory B cells (Table 3).

Example 3 Binding Specificity of HIV Antibodies

The size of the antibody clones captured by 2CC-core bait differed widely ranging from 2-76 diversified members (Table 3). To determine whether the antibodies captured by the 2CC-core bind to the HIV spike, ELISAs were performed using YU2 gp120 on representative members of each expanded clone. All of the antibodies tested bound to gp120 (Table 3).

The site of antibody binding on the HIV spike was mapped using mutant proteins that interfere with either the CD4bs (gp120(D368R)), or the CD4-induced co-receptor binding site (CD4i, gp120(I420R)). As reported, X. Wu et al., Science 329, 856 (Aug. 13, 2010), VRC01 is classified as a CD4bs antibody since it is sensitive to the D368R mutation, but because of the proximity of the CD4i site, it also shows some sensitivity to the I420R mutation. NIH45-46, which is a VRC01 variant, and antibodies 3BNC60, 8ANC131, and 12A12 showed ELISA patterns that were similar to VRC01 (These clonal members were selected based on neutralizing activity, Table 3). Other clones, including 1B2530, and 8ANC195, were equally sensitive to both mutations and could not be classified precisely based solely on ELISA.

To determine whether the antibodies are polyreactive, ELISAs were performed on purified ssDNA, dsDNA, insulin, and LPS. 63% of the anti-2CC Core antibodies tested were polyreactive. It was concluded that the majority of the antibodies captured by the 2CC-bait recognize either the CD4bs or the CD4i site on gp120 and many are also polyreactive.

Example 4 Somatic Hypermutation

Somatic hypermutation is required for development of high affinity antigen binding and in some cases contributes to polyreactivity of anti-HIV antibodies. To test if this is the case for highly mutated 2CC-core specific antibodies, 4 representative antibodies were reverted to the corresponding germline. Reversion led to complete loss of antigen binding in ELISA for all 4 clones tested and to loss of polyreactivity.

Example 5 HIV Neutralization

HIV neutralizing activity was measured in standardized in vitro assays using an initial panel of 8 viruses including 3 tier 1 Clade A, B and C, and 5 tier 2 Clade B Env pseudovirus variants (M. S. Seaman et al., J Virol 84, 1439 (February, 2010)). The neutralizing activity of the antibodies was compared to VRC01 and purified serum IgG from the donors (FIG. 1A, Table 4 and FIG. 6 ). Antibodies showing high levels of neutralizing activity were further tested on a panel of 15 additional tier 2 Clade A, B, C, D, G, AG and AE Env pseudovirus variants (FIG. 1B, Table 5) including 5 viruses that are resistant to VRC01 (FIG. 1B and Table 5).

90% of all of the antibodies tested showed some neutralizing activity and 6 clones contained antibody variants that showed high levels of potency and breadth (FIGS. 1A, B and C and Tables 4 and 5). These clones were also the most abundant among those captured by the 2CC-bait in each of the four patients studied (Table 3). The most impressive of the new antibodies, 3BNC117 belonging to a clone with 76 members, showed an average IC₈₀ on a combined group of 14 tier 2 viruses of 0.5 μg/ml as compared to 1.8 μg/ml for VRC01 (FIG. 1C, Tables 4 and 5).

Only 4 of the 20 viruses tested were more sensitive to VRC01 than 3BNC117, whereas 14 were more sensitive to 3BNC117 including DU172.17 which is completely resistant to VRC01 but sensitive to 3BNC117 (FIGS. 1B and C). NIH45-46, a new variant of VRC01, is more potent than VRC01 on 15 of the 20 viruses tested but still less potent than 3BNC117 (FIGS. 1B and C and Tables 4, and 5).

There was substantial variation in neutralizing breadth and potency among the members of the 5 most potent neutralizing antibody clones. For example, 3BNC156, a variant of 3BNC117, neutralized only 2 of the viruses in the initial panel and at much higher concentrations than 3BNC117 (FIG. 1A and Table 4) and 3BNC55, another variant, was intermediate between the two showing activity against 6 viruses at an average IC₅₀ of 4 μg/ml (FIG. 1 and Table 4). Finally, the most active antibodies were highly hypermutated. The average number of mutations for the top 10 antibodies was 72 for V_(H) and 45 for V_(L), and this was associated with their breadth and potency (Tables 4 and 5). Reversion of the mutated residues to germline resulted in a complete loss of neutralizing activity for all of the antibodies tested.

Example 6 Identification of Diagnostic Peptides

The foregoing cloning strategy captured antibodies produced by antigen binding memory B cells, but circulating antibodies are not produced by these cells, and originate instead from plasma cells in the bone marrow. However, cognate antigen cannot be used as bait to capture plasma cells because they do not express surface Ig A. (Radbruch et al., Nat Rev Immunol 6, 741 (October, 2006)). In addition, the relationship between plasma cells in the bone marrow and circulating memory B cells is not defined precisely. To determine whether the antibodies cloned from memory B cells are also found in the bone marrow plasma cell compartment, CD138-expressing plasma cells were purified from paired bone marrow samples from 2 of the 4 individuals studied and used PCR to specifically amplify IgV_(H) genes for the more potent antibodies cloned from memory B cells in these individuals. The following were the clone specific primers for RU01: CTGCAACCGGTGTACATTCTCAAGTGCAACTGGTGC (FWRD) (SEQ ID NO. 584), CTGCAACCGGTGTACATTCTCAGGTCCATTTGTCACAG (FWRD), (SEQ ID NO. 585) TGCGAAGTCGACGCTGACGAGACAGTGACCTGC (REV) (SEQ ID NO. 586), TGCGAAGTCGACGCTGAAGAGACAATAATTTG (REV) (SEQ ID NO. 587), TGCGAAGTCGACGCTGACGAGACAATAACT (REV) (SEQ ID NO. 588) and for RU10: CTGCAACCGGTGTACATTTTCAGGGGCACTTGGTG (FWRD) (SEQ ID NO. 589), TGCGAAGTCGACGCTGAGGTGACGATGACCGTG (REV) (SEQ ID NO. 590). Members of the selected clones and large numbers of additional variants were readily identified in both patients.

To verify that these antibodies can also be found in serum, IgG purified from the serum of the same 2 and one additional individual were adsorbed on the 2CC-core bait and mass spectrometry was performed on the eluted IgG (FIG. 1D, FIG. 7 and FIGS. 10A-C). Diagnostic peptides were found for the highly active antibody variants in all cases (FIG. 7 , FIG. 10A-C). It was concluded that broad and potent anti-HIV antibodies cloned from memory B cells were also found in the bone marrow plasma cell compartment, and in the circulating IgGs of patients with high serum titers of broadly neutralizing antibodies.

Example 7 HIV Antibody Binding Characteristics

To determine whether antibody affinity to gp120 is related to neutralizing activity, the binding of the highly active antibodies, selected clonal relatives and germline reverted progenitors were compared using Surface Plasmon Resonance (SPR) (FIGS. 2A and B, FIG. 8 and Table 6).

The top neutralizing antibodies showed affinities (K_(A)) ranging from ≅10⁷-10¹² (M⁻¹) on YU2 gp140 trimers and ≈10⁷-10¹¹ (M⁻¹) on the 2CC-core (FIGS. 2A and B and Table 6). Consistent with their decreased neutralizing potency and breadth, 3BNC66, 3BNC156 and 3BNC55 displayed lower affinities on YU2 gp140 trimers than 3BNC117, but surprisingly, affinities to 2CC-core did not correlate with neutralizing activity (FIG. 1 , FIG. 8 , Table 4 and Table 6). Binding by SPR was not detected for any of the germline reverted antibodies tested (FIG. 2B, Table 6). It was concluded that the anti-HIV antibodies captured by the YU2 2CC-core tended to show higher affinity to the corresponding gp140 trimer than to the 2CC-core.

When VRC01 binds to the HIV spike it produces large conformational changes that mimic CD4 binding and expose the CD4i site. By contrast, b12 and most other known anti-CD4bs antibodies do not.

To determine whether this is a shared feature of the highly active antibodies, HIV-BAL.26Δc or -YU2 gp160Δc was expressed on the surface of HEK 293T cells and CD4i antibody binding measured in the presence or absence of CD4 or anti-CD4bs antibodies (FIG. 2C). With one exception, all of the highly active antibodies tested resembled CD4 and VRC01 in that they facilitated anti-CD4i antibody binding to either HIV-BAL.26 or YU2 gp160Δc or both (FIG. 2C).

The only highly active antibody that did not share this characteristic, 8ANC195, was not a traditional anti-CD4bs antibody in that it was equally sensitive to the D368R and I420R mutations (Table 3). In addition, it differed from the other highly active antibodies in its neutralization pattern: it did not neutralize any of the tier 1 viruses and showed potent activity against H086.8, a Glade B virus resistant to all other antibodies tested including 3BNC117, VRC01 and b12 (FIGS. 1 A and B and Tables 4 and 5).

Example 8 HIV Antibody Sequence Identity

To determine whether highly active anti-CD4bs antibodies share common sequence features, the 10 best antibodies: 2 variants each from 5 independently derived antibody clones from 5 different patients were aligned (FIG. 3 ). Comparison of the IgV_(H) regions revealed a highly conserved consensus sequence covering 68 IgV_(H) residues (FIG. 3A). The IgV_(H) consensus included 6 of VRC01-gp120 contact residues, including VRC01-Arg 71, which mimics the key interaction of Arg59_(CD4) and Asp368_(gp120) (FIG. 3A). Moreover, the consensus, including the 6 contact residues, was entirely conserved in both of the closely related germline IgV_(H) genes (V_(H)1-2 and V_(H)1-46) that give rise to all of the antibodies in this class (FIGS. 3A and B).

The codons encoding the consensus residues were highly somatically mutated in the 10 selected antibodies, nevertheless the amino acid sequence was conserved (FIG. 9 ). The ratio of replacement to silent mutations in the consensus residues ranged from 0.7-1.7, whereas it was 3.5-22 in the non-consensus residues indicating that conservation of the consensus is strongly selected (Table 7). In contrast to the heavy chain, the light chain of VRC01 made only 8 out of a total of 32 contacts with gp120. Consistent with its more limited role, comparison of the light chain sequences of the same antibodies uncovered a less extensive consensus covering 53 IgV_(L) residues including 3 VRC01-gp120 contact residues (FIG. 3B). Finally, like the heavy chains, the light chains arose from a limited set of germline genes: 2 were derived from IgK1D-33, 2 from IgK3-11, and one from IgL1-47 (FIG. 3B and Table 3). Antibody 8ANC195, which differed from the others in several important respects did not entirely conform to the consensus and did not arise from related heavy or light chains (FIGS. 3A and B) It was concluded that there is significant sequence convergence among highly active agonistic anti-CD4bs antibodies (HAADs).

Example 9 Crystal Structure of 3BNC60 Fab

To determine whether the structure of the antibodies in different patients is also conserved, the crystal structure of the 3BNC60 Fab was solved to 2.65 Å resolution and compared it to VRC01. The structure revealed the four domains, V_(H), C_(H)1, V_(L), and C_(L), of a canonical Fab and the complementarity-determining regions (CDRs) within V_(H) and V_(L) that form the antigen binding site. The two Fabs in the 3BNC60 asymmetric unit were almost identical; however, the conformation of residues 74-78 in the loop connecting strands D and E varied slightly due to different chemical environments formed by crystal lattice contacts.

Superimposition of the V_(H) domains from 3BNC60 and VRC01 in the VRC01-gp120 co-crystal structure (T. Zhou et al., Science 329, 811 (Aug. 13, 2010)) yielded a root mean square deviation (rmsd) of 1.3 Å (calculated for 111 Ca atoms) with major differences confined to CDR2 residues 58-65 (3BNC60 numbering). Superimposing the structures indicated conservation of the recognition interface with gp120. For example, Arg72_(3BNC60) adopted a similar conformation as Arg71_(VRC01), which mimics an important salt bridge normally formed between Arg59_(CD4) and Asp368_(gp120). In addition, Trp47_(3BNC60) adopted the same conformation as Trp47_(VRC01), a residue that contacts gp120 and is involved with a complex network of interactions of aromatic and aliphatic residues that stabilize the conformations of CDRH3 and CDRL3. Gln65_(3BNC60), which corresponds to Gln64_(VRC01), is within the residue segment (residues 58-65) that differs in structure from VRC01. The conformation of this region of 3BNC60, which is involved in a lattice contact in the crystals, is likely to change upon binding gp120, as it would clash with the CD4-binding loop on gp120.

Superimposing the 3BNC60 and VRC01 V_(L) domains yielded an rmsd of 0.9 Å (calculated for 95 Cα atoms) and showed that some of gp120-contacting residues are structurally conserved; Tyr91_(3BNC60) and Glu91a_(3BNC60) adopted similar conformations as Tyr91_(VRC01) and Glu96_(VRC01), which engaged loop D of gp120 via polar interactions. Overall, these structural comparisons suggested that 3BNC60 binds gp120 with the same architecture as observed for the binding of VRC01.

Example 10 HIV Antibody Consensus Sequence

The foregoing experiments defined a class of agonistic anti-CD4bs antibodies, HAADs, that shares IgV_(H) and IgV_(L) consensus sequences including 8 of the contact residues between VRC01 and the HIV spike (FIGS. 3A and B). In five different donors, selected for their high level serologic anti-HIV activity, these antibodies originated from only 2 closely related IgV_(H) and 3 IgV_(L) germline genes that conform to the HAAD consensus: V_(H)1-2 and V_(H)1-46 differ by only 7 amino acids, none of which are part of the consensus (FIG. 3A). Despite extensive somatic hypermutation, the consensus residues were retained in their germline form.

The only exception to the consensus, 8ANC195, differed from the others in a number of ways that suggest that it may have a unique mode of antigen recognition: absence of the Arg in the heavy chain that mimics the critical Arg59_(CD4) and Asp368_(gp120) contact site; unique neutralizing pattern; and inability to facilitate anti-CD4i antibody binding. This antibody is one of two distinct highly active antibodies arising in one patient, lending additional support to the idea that serologic neutralizing activity is combinatorial.

TABLE A Seq Heavy Chain ID Amino Acid No. Antibody Sequence   5 8A253HC QGQLVQSGGGLKKPGTSVTISCLASEYTFNEFVIHWIRQAPGQGPLWLG LIKRSGRLMTAYNFQDRLSLRRDRSTGTVFMELRGLRPDDTAVYYCARD GLGEVAPDYRYGIDVWGQGSTVIVTAASTKG   6 8A275HC QGLLVQSGGGVKKLGTSVTISCLASEYTFNEFVIHWIRQAPGQGPLWLG LIKRSGRLMTSYQFQDRLSLRRDRSTGTVFMELRGLRVDDTAVYYCARD GLGEVAPAYLYGIDAWGQGTTVIVTSASTKG   7 8ABM11 FQGHLVQSGGGVKKPGTSVTLSCLASEYTFTEFTIHWIRQAPGQGPLWL GLIKRSGRLMTSYRFQDRLSLRRDRSTGTVFMELRSLRTDDTAVYYCAR DGLGELAPAYHYGIDAWGQGTTVIVTSASTS   8 8ABM12 QGHLVQSGGGVKKLGTSVTISCLASEYTFNEFVIHWIRQAPGQGPLWLG LIKRSGRLMTSYQFQDRLSLRRDRSTGTVFMELRGLRVDDTAVYYCARD GLGEVAPAYLYGIDAWGQGTTVIVTSAST   9 8ABM13 QGHLVQSGGGVKKLGTSVTISCLASEDTFNEFVIHWIRQAPGQGPLWLG LIKRSGRLMTSYQFQDRLSLRRDRSTGTVFMELRGLRVDDTAVYYCARD GLGEVAPAYLYGIDAWGQGTTVIVTSASTS  10 8ABM14 GHLVQSGGGXKKPGTSVTISCLASEYTFTEFTIHRIRQAPGQGPLWLGLI KGSGRLMTSYGFQDRLSLRRDRSTGTVFMELRSLRTDDTAVYYCARDG LGELAPAYHYGIDVWGQGTTVIVTSASTS  11 8ABM20 GVHFQGHLVQSGGGVKKPGSSVTISCLASEYTFTEFTIHWIRQAPGQGP LWLGLIKRSGRLMTSYRFQDRLSLRRDRSTGTVFMELRGLRIDDTAVYY CARDGLGEVAPAYLYGIDVWGQGTTVIVTSASTS  12 8ABM24 FQGQLVQSGGGVKKPGSSVTISCLASEYTFTEFTIHWIRQAPGQGPLWL GLIKRSGRLMTSYGFQDRLSVRRDRSTGTVFMELRSLRTDDTAVYYCAR DGLGELAPAYHYGIDVWGQGTTVIVTSASTS  13 8ABM26 QGQLVQSGGGVKKLGTSVTISCLASEYTFNEFVIHWIRQAPGQGPLWLG LIKRSGRLMTSYQFQDRLSLRRDRSTGTVFMELRGLRVDDTAVYYCARD GLGEVAPAYLYGIDAWGQGTTVIVTSASTS  14 8ABM27 QGHLVQSGXEVKKPGSSVKVSCKASGGTFSXYAIGWVRQAPGQGLEW MGGIIPILGTTNYAQRFQGGVTITADESTNTAYMDVSSLRSDDTAVYYCA KAPYRPRGSGNYYYAMDVWGQGTTVIVSSASTS  15 8ANC105HC QGHLVQSGGGVKKLGTSVTISCLASEYTFNEFVIHWIRQAPGQGPLWLG LIKRSGRLMTSYQFQDRLSLRRDRSTGTVFMELRGLRVDDTAVYYCARD GLGEVAPAYLYGIDAWGQGTTVIVTSASTKG  16 8ANC116HC QGQLVQSGGGVKKLGTSVTISCLASEYTFNEFVIHWIRQAPGQGPLWLG LIKRSGRLMTSYQFQDRLSLRRDRSTGTVFMELRGLRVDDTAVYYCARD GLGEVAPAYLYGIDAWGQGTTVIVSSASTKG  17 8ANC127HC QGHLVQSGGGVKKLGTSVTISCLVSEYTFNEFVIHWIRQAPGQGPLWLG LIKRSGRLMTSYQFQDRLSLRRDRSTGTVFMELRGLRVDDTAVYYCARD GLGEVAPAYLYGIDAWGQGTTVIVTSASTKG  18 8ANC131HC QGQLVQSGGGLKKPGTSVTISCLASEYTFNEFVIHWIRQAPGQGPLWLG LIKRSGRLMTAYNFQDRLRLRRDRSTGTVFMELRGLRPDDTAVYYCARD GLGEVAPDYRYGIDVWGQGSTVIVTAASTKG  19 8ANC134HC QGQLVQSGGGVKKPGTSVTISCLASEYTFNEFVIHWIRQAPGQGPVWLG LIKRSGRLMTSYKFQDRLSLRRDRSTGTVFMELRGLRLDDTAVYYCARD GLGEVAPAYLYGIDAWGQGSTVIVTSASTKG  20 8ANC13HC QGQLVQSGGGVKKPGASVTISCLASEYTFNEFVIHWIRQAPGQGPLWLG LIKRSGRLMTAYKFQDRLSLRRDRSTGTVFMELRGLRPEDTAVYYCARD GLGEVAPDYRYGIDVWGQGSTVIVSAASTKG  21 8ANC171HC QGHLVQSGGGVKKLGTSVTISCLASEYTFNEFVIHWIRQAPGQGPLWLG LIKRSGRLMTSYQFQDRLSLRRDRSTGTVFMELRGLRVDDTAVYYCARD GLGEVAPAYLYGIDAWGQGTTVIVTSASTKG  22 8ANC18 GVHFQGHLVQSGGGVKKPGSSVTISCLASEYTFTEFTIHWIRQAPGQGP LWLGLIKRSGRLMTSYRFQDRLSLRRDRSTGTVFMELRGLRIDDTAVYY CARDGLGEVAPAYLYGIDVWGQGSTVIVTSASTS  23 8ANC182HC QGQLVQSGGGVKKPGTSVTISCLASEYTFTEFTIHWIRQAPGQGPLWLG LIKRSGRLMTAYRFQDRLSLRRDRSTGTVFMELRNLRMDDTAVYYCARD GLGELAPAYQYGIDVWGQGTTVIVSSASTKG  24 8ANC192HC QGHLVQSGGGVKKLGTSVTISCLASEYTFNEFVIHWIRQAPGQGPLWLG LIKRSGRLMTSYQFQDRLSLRRDRSTGTVFMELRGLRVDDTAVYYCARD GLGEVAPAYLYGIDAWGQGTTVIVTSASTKG  25 8ANC22HC QGHLVQSGGGVKKLGTSVTISCLASEDTFNEFVIHWIRQAPGQGPLWLG LIKRSGRLMTSYQFQDRLSLRRDRSTGTVFMELRGLRVDDTAVYYCARD GLGEVAPAYLYGIDAWGQGTTVIVTSASTKG  26 8ANC26HC QGQLVQSGGGVKKPGTSVTISCLASEYTFNEFVIHWIRQAPGQGPVWLG LIKRSGRLMTSYKFQDRLSLRRDRSTGTVFMELRGLRLDDTAVYYCARD GLGEVAPAYLYGIDAWGQGSKVIVTPASTKG  27 8ANC2HC QGQLVQSGGGVKKLGTSVTIPCLASEYTFNEFVIHWIRQAPGQGPLWLG LIKRSGRLMTSYQFQDRLSLRRDRSTGTVFMELRGLRVDDTAVYYCARD GLGEVAPAYLYGIDAWGQGTTVIVTSASTKG  28 8ANC30HC QGQLVQSGGGVKKLGTSVTISCLASEYTFNEFVIHWIRQAPGQGPLWLG LIKRSGRLMTSYQFQDRLSLRRDRSTGTVFMELRGLRVDDTAVYYCARD GLGEVAPAYLYGIDAWGQGTTVIVTSASTKG  29 8ANC37HC QGHLVQSGGGVKKLGTSVTISCLASEYTFNEFVIHWIRQAPGQGPLWLG LIKRSGRLMTSYQFQDRLSLRRDRSTGTVFMELRGLRVDDTAVYYCARD GLGEVAPAYLYGIDAWGQGTTVIVTSASTKG  30 8ANC40HC QGHLVQSGGGVKKLGTSVTISCLASEYTFNEFVIHWIRQAPGQGPLWLG LIKRSGRLMTSYQFQDRLSLRRDRSTGTVFMELRGLRVDDTAVYYCARD GLGEVAPAYLYGIDAWGQGTTVIVTSASTKG  31 8ANC41HC QGQLVQSGGGVKKTGTSVTISCLASEYTFTEFTIHWIRQAPGQGPLWLG LIKRSGRLMTANRFQDRLSLRRDRSTGTVFMELRSLRIDDTAVYYCARD GLGELAPAYHYGIDVWGQGTTIIVTSASTKG  32 8ANC45HC QGQLVQSGGGVKKTGTSVTISCLASEYTFTEFTIHWIRQAPGQGPLWLG LIKRSGRLMTANRFQDRLSLRRDRSTGTVFMELRSLRIDDTAVYYCARD GLGELAPAYHYGIDVWGQGTTIIVTSASTKG  33 8ANC50HC QGQLVQSGGGVKKPGTSVTISCLASEYTFTEFTIHWIRQAPGQGPLWLG LIKRSGRLMTAYRFQDRLSLRRDRSTGTVFMELRNLRMDDTAVYYCARD GLGELAPAYQYGIDVWGQGTTVIVSSASTKG  34 8ANC53HC QGQLVQSGGGGKKLGTSVTISCLASEYTFNEFVIHWIRQAPGQGPLWLG LIKRSGRLMTSYQFQDRLSLRRDRSTGTVFMELRGLRVDDTAVYYCARD GLGEVAPAYLYGIDAWGQGTTVIVSSASTKG  35 8ANC88HC QGQLVQSGGGVKKPGTSVTISCLASEYTFNEFVIHWIRQAPGQGPLWLG LIKRSGRLMTSYKFQDRLNLRRDRSTGTVFMELRGLRPDDTAVYYCARD GLGEVAPDYRYGIDVWGQGSTVIVTAASTKG  36 8ANC103HC QVQLQQWGSGLLKPSETLSLTCAVYGGSFRSYYWNWIRQSPGKGLEWI GEVSHSGSTNYNPALKSRVTISVDTSKNQFSLKVKSVTAADTALYYCSR GRGKRCSGAYCFAGYFDSWGQGGLVWSSASTKG  37 8ANC106HC EVQLVESGGGVVEPGESLRLSCAASGFTFRSYDMFWVRQATGKSLEW VSAIGIAGDTYYSGSVKGRFTISRENARTSLYLQLSGLRVEDSAVYFCVR GSPPRIAATEYNYYYGLDVWGQGTTVSVFSASTKG  38 8ANC107HC VVQLVQSGAEVRKPGSSLKVSCKSSGGTFSRYVVNWVRQAPGQGLEW MGGMIPIFGIAKYAQKFQDRVTMTADESKNTVYLDFSSLRSDDTAVYYCA RDRGDTRLLDYGDYEDERYYYGMDVWGQGTTVIVSSASTKG  39 8ANC108HC QVQLVQSGAEVRKPGSSLKVSCKSSGGTFSRYVVNWVRQAPGQGLEW MGGIIPIFGIAKYAQKFQDRVTMTADEPKNTVYLDFNSLRSDDTAVYYCA RDRGDTRLLDYGDYEDERYYYGMDVWGQGTTVIVSSASTKG  40 8ANC109HC EVQLVESGGGLVKPGGSLRLSCAASGFSFSEHYMSWIRLAPGKGLEWL SYISSSTRTTYSADSVRGRFTISRDTAKQLLFLHMSSLRAEDTAVYYCVR LYGGINGWFDQWGQGTLVSVSSASTKG  41 8ANC10HC QVQLVQSGAEVKKPGSSVKVSCKTSGGSFSNYAFSWVRQAPGEGLEW MGRIIPIFGTAKYTQKLQGRVTITADKFTSTVYMELSSLRSEDTAIYYCASL HQGPIGYTPWHPPPRAPLGQSVCG  42 8ANC111HC QVQLVESGAEVKKPGASVKVSCKASGYTFTSHDINWRQATGQGLEW MGWMNPNSGDTGYAHKFQGRVTMTRNTPISTAYMELSSLRSEDTAVYY CARGRATSRNTPWAHYYDSSGYYGAGDYWGQGTLVTVSSASTKG  43 8ANC112HC QVQLVESGGGVVQPGRSLRLFCAASGFAFNTYGMHWVRQAPGKGLEW VAVTWHDGSQKYYADSVKGRFTISRDNSKNTLYLQMNSLRAEDTAIYYC ASDQGGFDDSSGYFAPGGMDVWGRGTTVIVSSAPTKG  44 8ANC113HC QVQLVESGAELRKPGESLEISCKASGYSFSSHWIGWARQMPGKGLEWM GIIYPGDSNTIYSPSFQGQVTISADKSINTAYLQWSSLKASDTAMYFCASN YHDYFYWGQGTLVTVSSASTKG  45 8ANC114HC EVQLVESGAEVKKPGSSVKVSCKASGGTFSTYAFSWVRQAPGQGLEW MGGIIPIFGTENYAQKFQGRVTITADKSTSTAYMELSSLRSEDTAVYYCA RDRSSAIGYCSSISCYKGSFDIWGQGTMVTVSSASTKG  46 8ANC115HC QVQLVQSGAEVRKPGSSLKVSCKSSGGTFSRYVVNWVRQAPGQGLEW MGGIIPIFGIAKYAQKFQDRVTMTADEPKNTVYLDFNSLRSDDTAVYYCA RDRGDTRLLDYGDYEDERYYYGMDVWGQGTTVIVSSASTKG  47 8ANC117HC EVQLVQSGAEVKKPGSSVKVSCKASGGTFSTYAFSWVRQAPGQGLEW MGGIIPIFGTENYAQKFQGRVTITADKSTSTAYMELSSLRSEDTAVYYCA RDRSSAIGYCSSISCYKGSFDIWGQGTMVTVSSASTKG  48 8ANC11HC QVFVQLVQSGGGLVQPGGSVRLSCTASGFLFSTYSMNWVRQAPGKGL EWVSSISTTSNYIYYADSVKGRFTISRSNGQGSLYLQLNSLRVEDTAVYY CARDTKVGAPRQDCYAMDLWGQRDHGHRLLSFHQGPIGLPPGALLQ  49 8ANC121HC QVQLLESGPGLVTPSGTLSLACAVSGASISSSHWWTWVRQSPGKGLEW IGEIDRRGTTNYNPSLRSRVTILLDNSKNQFSLSLRSVTAADTAVYYCTKV YAGLFNERTYGMDVWGHGTTVLVSSASTKG  50 8ANC126HC QVQLVESGAEVRKPGSSLKVSCKSSGGTFSRYVVNWVRQAPGQGLEW MGGIIPIFGIAKYAQKFQDRVTMTADESKNTVYLDFSSLRSDDTAVYYCA RDRGDTRLLDYGDYEDERYYYGMDVWGQGTTVIVSSASTKG  51 8ANC130HC QVQLLQSGAEVKKPGASVKVSCKVSGYTLTELSINWVRQAPGKGLEWM GGFDPEDDEAIYEPKFQGRLTMTEDTSTDTAYMELSSLRSEDTAVYYCA TADPFKVAQDEGLYVIFDYWGQGTLVTVSSASTKG  52 8ANC132HC QVQLVQSGTEVQKPGASVKVSCKTSGYTFSKYYIHWVRQAPGQGLEWV GRINTDSGGTDYAEKFQGRVTMTRDTSITTVYLEMRGLTSDDTAAFYCA RGPPHAGGWTIYYYGLDVWGQGTSVIVSSASTKG  53 8ANC133HC QVQLVQSGAEVKKPGASVKVSCKVSGHTLSELSINWRHVPGKGLEWM GGLDPEDGEAIHEPKFQGRLTMTEDTSTDTAYVELSSLRSEDTAMYYCA TADPFKVAQDEGLYVIFDYWGQGTLVTVSSASTKG  54 8ANC136HC EVQLVESGGGVVQPGRSLRLSCAASGFTFSHHGIHWVRQAPGEGLEW VAVISEDGTNIHYEDSVRGRFTISRDNSKNTVDLQMNSLRAEDTAVYYCA SLISMRDGDAFDLWGQGTRVTVSSASTKG  55 8ANC137HC QVQLVQSGAEVRKPGSSLKVSCKSSGGTFSRYVVNWVRQAPGQGLEW MGGIIPIFGIAKYAQKFQDRVTMTADESKNTVYLDFSSLRSDDTAVYYCA RDRGDTRLLDYGDYEDERYYYGMDVWGQGTTVIVSSASTKG  56 8ANC139HC QVQLVQSGGGLVKPGGSLRLSCAASGFTFSSYSMNWVRQAPGKGLEW VSSISSSSSYIYYADSVKGRFTISRDNAKNSLYLQMNSLRAEDTAVYYCA REGSYYYGMDVWGQGTTVTVSSASTKG  57 8ANC140HC EVQLVQSGGGLVQPGRSLRLSCAASGFTFDDYAMHWVRQAPGKGLEW VSGISWNSGTIGYADSVRGRFTISRDDAKSSLYLQMNSLRTEDTALYYCA KDGWVGSGSSTLRGSDYWGQGTLVTVSSASTKG  58 8ANC142HC QIHLVQSGTDVKKPGSSVTVSCKAYGVNTFGLYAVNWVRQAPGQSLEYI GQIWRWKSSASHHFRGRVLISAVDLTGSSPPISSLEIKNLTSDDTAVYFC TTTSTYDQWSGLHHDGVMAFSSRGQGTLISVSAASTKGPSVFPLAPSSK STYGLAHVL  59 8ANC143HC QVQLVQSGAEVRKPGSSLKVSCKSSGGTFSRYVVNWVRQAPGQGLEW MGGIIPIFGIAKYAQKFQDRVTMTADEPKNTVYLDFNSLRSDDTAVYYCA RDRGDTRLLDYGDYEDERYYYGMDVWGQGTTVIVSSASTKG  60 8ANC144HC QLQLQESGPGLVKPWETLVLTCSVSGGSISSGDYYWGWIRQSPGKGPE WIGNIFYSSGNTYYNTSLKSRVTISVDVSKNRFSLKLTSMTAADTAVYYC GRLSNKGWFDPWGQGTLVSVSSASTKG  61 8ANC145HC QVQLLESGGGLVQRGGSLRLSCTASGFVFNNYWMTWVRQAPGNGLE WVANIDQDGSEKHYLDSVKGRFTISRDNAKNSLYLQMNSLRAEDTAIYY CARVRFKVTAWHRFDSWGQGDLVTVSSTSTKG  62 8ANC146HC LVQLLQSGAEVKKPGASVKVSCKVSGYTLTELSIHWVRQAPGKGLEWM GGFDPEDDEAIYEPKFQGRLTMTEDTSTDTAYMELSSLRSEDTAVYYCA TADPFKVAQDEGLYVIFDYWGQGTLVTVSSASTKG  63 8ANC147HC QVQLVESGGGLGQPGGSLRLSCAASGFTFRNYAMSWVRQAAGKGLEW VSGVSGGGDTTYYGDSVKGRFTISRDNSKNTLYLQMNNLRAEDTAVYY CAKDKGVWGSSDFDYWGQGTLVTVSSASTKG  64 8ANC148HC QVHLVQSGAEVKKPGASVRVSCKASGYTFTTYGISWVRQAPGQGLEW MGWISAHSGDTNYAQKLQARVTMTTDTSTNTAYMELRSLTSDDTAVYY CARDRPRHYYDRGGYYSPFDYWGQGTLVTVSSASTKG  65 8ANC149HC QVQLVESGAEVKKPGSSVKVSCKASGGTFNIFAFSWVRQAPGQGLEW MGGIIPIFASPNYAQRFQGRVTITADESTSTVHMELSSLRSEDTAIYYCAK DAHMHIEEPRDYDYIWGTSPYYFDYWGQGTLVTVSSASTKG  66 8ANC14HC QVQLVQSGAEVKKPGASVKVSCKVSGYTLTELSIHWVRQAPGKGLEWM GGFDSEDGEAFYKQNFQGRVTMTEDTSTDTAYMELRRLRSEDTAVYYC ATADRFKVAQDEGLFVIFDYWGQGTLVTVSSASTKG  67 8ANC150HC QVQLLQSGGEVKKPGASVKVSCKVSGYTLTELSIHWVRQAPGKGLEWM GGFDPEDDEAIYEPKFQGRLTMTEDTSTDTAYMELSSLRSEDTAVYYCA TADPFKVAQDEGLYVIFDYWGQGTLVTVSSASTKG  68 8ANC151HC EVQLVESGGGLVQPGGSLRLSCAASGFTFSSYSMNWVRQAPGKGLEW VSYISGSSYTIYYADSVRGRFTISRDNAKNSLYLQMNSLRDEDTAVYFCA RATPPNPLNLYNYDSSGSSFDYWGQGTLVTVSSASTKG  69 8ANC153HC QVQLVQSGAEVRKPGSSLKVSCKSSGGTFSRYVVNWVRQAPGQGLEW MGGMIPIFGIAKYAQKFQDRVTMTADESKNTVYLDFSSLRSDDTAVYYCA RDRGDTRLLDYGDYEDERYYYGMDVWGQGTTVIVSSASTKG  70 8ANC154HC QVQLVESGAEVRKPGSSLKVSCKSSGGTFSRYVVNWVRQAPGQGLEW MGGIIPIFGIAKYAQKFQDRVTMTADEPKNTVYLDFNSLRSDDTAVYYCA RDRGDTRLLDYGDYEDERYYYGMDVWGQGTTVIVSSASTKG  71 8ANC155HC QVQLVQSGAEIKKPGESLKISCKASGYTFNDYWIGWVRQMPGKGLEWM GIFYPDDSDSNYSPSFQGRVTISADKSITTAYLQWSTLKASDSAMYFCAR LLGDSGAFDIWGQGTMVIVSSASTKG  72 8ANC156HC EVQLVESGAEVRKPGSSLKVSCKSSGGTFSRFWNWVRQAPGQGLEW MGGMIPIFGIAKYAQKFQDRVTMTADESKNTVYLDFSSLRSDDTAVYYCA RDRGDTRLLDYGDYEDERYYYGMDVWGQGTTVIVSSASTKG  73 8ANC157HC QVQLVQSGAEVKKPGSSVKVSCKASGGTFSTYAFSWRQAPGQGLEW MGGIIPIFGTENYAQKFQGRVTITADKSTSTAYMELSSLRSEDTAVYYCA RDRSSAIGYCSSISCYKGSFDIWGQGTMVTVSSASTKG  74 8ANC158HC QVQLVQSGAEVRKPGSSLKVSCKSSGGTFSRFWNWVRQAPGQGLEW MGGMIPIFGIAKYAQKFQDRVTMTADESKNTVYLDFSSLRSDDTAVYYCA RDRGDTRLLDYGDYEDERYYYGMDVWGQGTTVIVSSASTKG  75 8ANC160HC QVQLVQSGGGVVQPGRSLRLSCAASGFTFSHHGIHWVRQAPGEGLEW VAVISEDGTNIHYEDSVRGRFTISRDNSKNTVDLQMNSLRAEDTAVYYCA SLISMRDGDAFDLWGQGTRVTVSSASTKG  76 8ANC161HC EVQLVQSGGGLVKPGGSLRLSCAASGFTFKNAWMSWVRQAPGKGLEW VGHIKSKTDGGTIDYAAPVKGRFTISRDDSKNTLYLQMNSLKIEDTAVYYC TTDIGSGRGWDFHYYDSNDWGQGTLVTVSSASTKG  77 8ANC162HC EVQLVQSGGGVVQPGRSLRLSCVVSGFTFSSFTFHWVRQAPGKGLEW VAGMSFHATYIYYADSVKGRFTISRDDSQDTLYLEMDSLRSEDTAIYYCA RDPGIHDYGDYAPGAFDYWGQGSPVTVSSASTKG  78 8ANC163HC LVQLVQSGAEVKKPGASVKVSCKVSGHTLSELSINWVRHVPGKGLEWM GGLDPEDGEAIHEPKFQGRLTMTEDTSTDTAYSTLSVWAPVAAAMYYCA TADPFKVAQDEGLYVIFDYWGQGTLVTVSSASTKG  79 8ANC164HC EVQLVESGAEVKKPGSSVKVSCKASGGTFSSYSISWVRQAPGQGLEW MGGIIPIFATTHYGQKFQGRIKITADKSTSTAYMELSRLRSEDTAVYYCAR DREFYFYGMDVWGQGTTVTVSSASTKG  80 8ANC165HC QVQLQQWGAGLLKPSETLSLTCAVYAGSFSGYYWTWIRQPPGKGLEWI GEVNHGGSTNYNPSLKSRVTLSVDTSKNQFSLKLTSVTAADTAVYYCAR VSRYDFWSGNYGSYGLDVWGQGTTVTVSSASTKG  81 8ANC166HC VVQLVQSGAEVRKPGSSLKVSCKSSGGTFSRFWNWVRQAPGQGLEW MGGMIPIFGIAKYAQKFQDRVTMTADESKNTVYLDFSSLRSDDTAVYYCA RDRGDTRLLDYGDYEDERYYYGMDVWGQGTTVIVSSASTKG  82 8ANC168HC LVQLVQSGAEVKKPGASVKVSCKVSGYSLTELSIHWVRQAPGKGLEWM GGFDSEDGEAIYKQNFQGRVTMTEDTSTDTAYMELSRLRSEDTAVYYC ATADPFKVAQDEGLFVIFDYWGQGTTGHRLLSLHQGPHRLYSLGTLLSR APIVQTHMA  83 8ANC169HC QVQLVQSGAEVKKPGSSVKVSCKASGGTFSTYAFSWVRQAPGQGLEW MGGIIPIFGTENYAQKFQGRVTITADKSTSTAYMELSSLRSEDTAVYYCA RDRSSAIGYCSSISCYKGSFDIWGQGTMVTVSSASTKG  84 8ANC16HC QVQLVQSGAEVKKPGSSVKVSCKASGGTFSTYAFSWVRQAPIEGLEWM GGIIPIFGTENYAQKFQGRVTITADKSTSTAYMELSSLRSEDTAVYYCARD RSSAIGYCSSISCYKGSFDIWGQGTMVTVSSASTKG  85 8ANC173HC QVQLVQWGAGLLKPLETLSLTCAVYGGSFNGYFWSWIRQTPGKGLEWI GEINHGGSANFNPSLKSRVTMSVDTSKNQFSLKLASVTAADTAIYYCAR GRITMVRGDPQRGGVRMDVWGQGTSVTVSSASTKG  86 8ANC174HC QVQLMQSGAEVKRPGASVKVSCKAFRHSLNNLGISWIRRAPGRGLEWL GWINVYEGNTKYGRRFQGRVTMTTDRSTNTVSMELRSLTSDDTAVYYC ARDNHFWSGSSRYYYFGMDVWGQGTTVIVSSASTKG  87 8ANC175HC QVQLVQSGGGLVQPGESLRLSCTASGFTFSSYNMNWVRQAPGKGLEW ISYISDKSKNKYYADSVRGRFTISRDNAQNSLFLQMSSLRDEDTAVYYCT REGPQRSFYFDYWGQGIQVTVSSASTKG  88 8ANC176HC QVQLQESGPGLVKPSETLSLTCTVSGGSISNHYWSWIRQPPGKGLEWIG YIYHSGNINYKSSLKSRATISIDTSNNQFSLKLSSVIAADTAVYYCARNFGP GSPNYGMDVWGQGTTVTVSSASTKG  89 8ANC177HC VVQLVQSGPGLVKPSQTLSLTCTVSGGSISSGDFYWSWIRQPPGKGLE WIGYIYYSGSTYYNPSLKSRLTISVDTSKNQFSLRLSSVTAADTAVYYCAR DLNSRIVGALDAFDIWGQGTMVTVSSASTKG  90 8ANC178HC QVQLVESGGALVQPGGSLRLSCAASGFSFSSYAMSWVRQAPGKGLEW VSAISRSGGSTYYADSVKGRFTISIDNSNNTLYLQMNSLRVEDTAVYYCA KREAFYYGAGGYGMDVWGQGTTVTVSSASTKG  91 8ANC179HC EVQLVESGGGLVKPGGSLRLSCEASGFTFTNAWMNWVRQAPGKGLEW VGRIKSQTHGGTTRYAAPVKGRFTISRDDSKHTLYLQMDRLTTEDTAVY YCTGTITGSTFYYYGMDVWGQGTTVTVSPASTKG  92 8ANC17HC EVQLVESGGGLLQPGGSLRLSCAASGFSFNDFEMNWVRQAPGKGLEW VSYISNDGTMIHYADSVKGRFTISRDNAKKSLFLQMNSLRAEDTAVYYCA RLAEVPPAIRGSYYYGMDVWGQGTTVTVASASTKG  93 8ANC180HC QVQLQESGPGLLRPLETLSLTCSVSGGSIRGYFWSWVRQPAGRGLEWI GRIYSSGTTRFNPSLKSRVRLSIDTAKSEVSLNITSVTAADSASYFCAGTS PVHGGLDLWGLGLRVTVSSASTKG  94 8ANC181HC HLVQSGTEVKKPGSSVTVSCKAYGVNTFGLYAVNWVRQAPGQSLEYIG QIWRWKSSASHHFRGRVLISAVDLTGSSPPISSLEIKNLTSDDTAVYFCTT TSTYDQWSGLHHDGVMAFSSWGQGTLISVSAASTKG  95 8ANC184HC EVQLVQSGAEVKKPGASVKVSCKVSGYTLTELSIHWVRQAPGKGLEWM GGFDPEDDEAIYEPKFQGRLTMTEDTSTDTAYMELSSLRSEDTAVYYCA TADPFKVAQDEGLYVIFDYWGQGTLVTVSSASTKG  96 8ANC185HC QVQLVESGGGLVQPGGSLRLSCAASGFTFSTHWMHWVRQAPGKGLV WVSRIHSDGRSTSYADSVKGRFTISRDNAKNTLYLQMNSLRAEDTAVYY CARGAAVFGVVIIGGMDLWGQGTTVTVSSASTKG  97 8ANC186HC EVQLVESGGGVVQPGGSLRLSCAASGFMFKNYAMHWVRQPPGKGLE WVAVIWYGGRDQNYADSVKGRFTISRDDSDNTLYLQMNSLRAGDTAVY FCARNSQVGRLMPAAGVWGQGTLVTVSSASTKG  98 8ANC187HC EVQLVESGGGLIQRGGSLRLSCVASGFPVSDNHMSWVRQAPGKGLEW VSIIYSDGGTYYADSVKGRFTISRDNSKNTVYLQMNSLRATDTAVYYCAR DPGFHYGLDVWGQGTTVTVSSASTKG  99 8ANC188HC VVQLVESGGGLVQPGGSLRLSCAASGFAFRSYWMSWVRQAPGRGLE WVANIKQDGSEKYYADSVKGRFTISRDNTKNSLYLQMNSLRAEDTAVFY CASRGDRYGPIDYWGQGTLVTVSSASTKG 100 8ANC191HC VVQLVESGTEVKKPGSSVKVSCKASGGTFSGSDISWVRQAPGQGLEW MGGIIPMFDIENHAEKFRGRLTITAVKSTGAAYMELSSLRSEDAAVYYCA RSSGNYDFAYDIWGQGTRVIVSSASTKG 101 8ANC193HC EVQLVQSGAEVKKPGSSVKVSCKASGGTFSTYAFSWVRQAPGQGLEW MGGIIPIFGTENYAQKFQGRVTITADKSTSTAYMELSSLRSEDTAVYYCA RDRSSAIGYCSSISCYKGSFDIWGQGTMVTVSSASTKG 102 8ANC194HC EVQLVQSGGGLVQPGGSLRLSCAASGLTFRNFAMSWVRQAPGKGLEW VSSISGSGGSTYYADSVKGRFTISRDNSKNTLYLQMNSLRGEDTAVYFC AKGVGYDILTGLGDAFDIWGQGTVVAVSSASTKG 103 8ANC195HC QIHLVQSGTEVKKPGSSVTVSCKAYGVNTFGLYAVNWVRQAPGQSLEYI GQIWRWKSSASHHFRGRVLISAVDLTGSSPPISSLEIKNLTSDDTAVYFC TTTSTYDKWSGLHHDGVMAFSSWGQGTLISVSAASTKG 104 8ANC196HC VVQLVQSGTEVKKPGSSVKVSCKASGGTFSGSDISWVRQAPGQGLEW MGGIIPMFDIEDHAQKFRGRLTITADKSTGAAYMELSSLRSEDAAVYYCA RSSGNYDFAFDIWGQGTRLIVSSASTKG 105 8ANC20HC QVQLGESGGGLVEPGGSLRLSCAASGFLFSDYQMSWIRLAPGKGLEWI SFISGFGSVYYADSVEGRFTISRDNARNSLYLQMNNLRAEDTAVYYCAR AYGTGNWRGLYYYYYGMDVWGHGTTVTVSSASTKG 106 8ANC21HC QLQLVESGGGVVQPGRSLRLSCAASGFTFSTYTMHWVRQAPGKGLEW VAVISYDGTNKYYADSVKGRFTISRDNSKNTLYLQMNSLRGEDTAVYYC ARSPSYYFDYWGQGTLVTVSAASTKG 107 8ANC24HC QVQLVQSGAEVKMPGASVKVSCKVSGYSLTELSIHWVRQAPGKRLEW MGGFDPEDDERIYAQKFQDRVTMTEDTSTDTAYMDLNSLRSEDTAVYY CTTGGLYCSSISCIMDVWGQGTTVIVSSASTKG 108 8ANC25HC QVQLVQSGAEVKKPGASVKVSCKVSGYTLTELSIHWVRQAPGKRLEWM GGFDPEDGERIYAQKFQGRVTMTEDTSTDTAYMELNSLRSDDTAVYYC ATGGLYCSSISCIMDVWGQGTTVTVSSASTKG 109 8ANC27HC QVQLVQSGAEVKKPGASVKVSCKVSGYTLTELSIHWVRQAPGKGLEWM GGFDSEDGEAIYKQNFQGRVTMTEDTSTDTAYMELSRLRSEDTAVYYC ATADRFKVAQDEGLFVIFDYWGQGNPGHRLLSLHQGPIGLPPGTLPPKA TSGHAARR 110 8ANC31HC QVQLVESGGGVVQPGRSLRLSCAASGFTFSSYAMHWVRQAPGKGLEW VAVISYDGSNKYYADSVKGRFTISRDDSKSTVYLQINSLRAADTAVYFCA REGGLRFLEWLFWGQGTLVTVSSGESSASTKG 111 8ANC33HC EFQLVQSGGGLVKPGGSLRLSCTGSTFSFSSDDMNWVRQAPGKGLEW VSSMSDSGSHIYYADFVKGRFTISRDNAKKSLYLQMNSLRAEDTAVYYC AQSRPPQRLYGMDVWGQGTTVTVSSASTKG 112 8ANC34HC QVQLVQSGAEVKKPGASVKVSCKVSGYTLTELSIHWVRQAPGKGLEWM GGFDPEDGEASFEPKFQGRLTMTEDTSTDTAYMELSSLRSEDTAVYYC ATADPFKVAQDEGLYVIFDYWGQGTLVTVSSASTKG 113 8ANC36HC QVQLVESGGGVVQPGKSLRLSCAASGFTFSTHAMHWVRQAPGKGLDW VAVISHDGDNQYYADAVKGRFTISRDDSRDTVFLQMNSLRTEDTGVYYC AADSSGSNWFDYWGQGILVTVSSASTKG 114 8ANC38HC EPMFQPGQSGGVVVQSGESLHLSCEASGFKFASQMMHWVRHVPGRG LEWVALISWDGSGKLFADSVRGRFTIHRWNDRNSLYLDVKNVRPEDAAI YYCTRNGFDVWGQGILVTVSSASTKG 115 8ANC39HC QVQLLQSGAEVKKPGASVKVSCKVSGYTLTELSIHWVRQAPGKGLEWM GGFDPEDDEAIYEPKFQGRLTMTEDTSTDTAYMELSSLRSEDTAVYYCA TADPFKVAQDEGLYVIFDYWGQGTLVTVSSASTKG 116 8ANC3HC QVHLQESGPRLVRSSETLSLTCSVPGGSIVNPITNYYWSWIRQSPRKGL QWIGDIYYTGTSSRNPSLDSRVSISMDVSRKQISLTLYSVTAADTAVHYC ASQSLSWYRPSGYFESWGQGILVTVSSASTKG 117 8ANC43HC QVQLVQSGAEVKKPGSSMKVSCKSSGGTFSNHAISWVRQAPGKGLEW MGGIIPMSGTTNYLQKFQGRVTITADEFATTAYMELSSLTSEDTAVYYCA RARADSHTPIDAFDIWGPGTRVIVSSASTKG 118 8ANC46HC QVQLVQSGTEVKKPGSSVKVSCKASGGTFSDSDIAWVRQAPGQGLEW MGGITPMFDMAKSAQKFRGRLIITADKSTGTAYMELSSLRYEDAAVYFCA RSSGNFEFAFEIWGQGTKIIVSLASTKG 119 8ANC48HC QVQLVQSGAEVKKPGASVKVSCKASGYTFTSYDINWVRQATGQGLEW MGWMNPNSGNTGYAQTFQGRVTMTRNTSISTAYMELSSLRSEDTAVYY CARDRWLPQYYYYGMDVWGQGTTVTVSSASTKG 120 8ANC49HC FVQLVESGGGLVQPGGSLRLSCAASGFNFNTYWMNWVRQAPGKGLEW VANMKEDGSEKYYVDSVKGRFTISRDNAKNSLYLQMNSLRAEDTAVYYC ARNPESRCIVGRNRGWCRYFDLWGRGSLVTVSPASTKG 121 8ANC51HC LVQLVESGGGVVQPGRSLRLSCAASGFTFSTYAMHWVRQAPGKGLEW VAVISYDGSNKFYADSVKGRFTISRDNSKNTLYLQMNSLRAEDTAVYYCA RPKFLPGADIWWVAATPFDYWGQGNPGHRLLSFHQGPIGLPPG 122 8ANC57HC PMFQPGQSGGWVQSGESLHLSCEASGFKFASQMMHWVRHVPGRGL EWVALISWDGSGKLFADSVRGRFTIHRWNDRNSLYLDVKNVRPEDAAIY YCTRNGFDVWGQGILVTVSSASTKG 123 8ANC58HC QVQLVQSGAEVKKPGASVKVSCKVSGHTLSELSINWVRHVPGKGLEWM GGLDPEDGEAIHEPKFQGRLTMTEDTSTDTAYVELSSLRSEDTAMYYCA TADPFKVAQDEGLYVIFDYWGQGTLVTVSSASTKG 124 8ANC5HC QVQLVQSGAEVRKPGSSLKVSCKSSGGTFSRFWNWVRQAPGQGLEW MGGMIPIFGIAKYAQKFQDRVTMTADESKNTVYLDFSSLRSDDTAVYYCA RDRGDTRLLDYGDYEDERYYYGMDVWGQGTTVIVSSASTKG 125 8ANC60HC LVQLVESGGGVVQPGKSLRLSCATSGFTFSTYGMHWVRQAPGKGLEW VAVIWYDGSYKYYADSVKGRFTISRDNSKNTLFLQMNSLRAEDTAMYYC GREMAVGGTKALDHWGQGTLVTVSSASTKG 126 8ANC63HC QVQLVQSGAEAKRPGDSVKVSCKASGYTFTEYYIHWVRQTPGQGFEW MGIITPGAGNTTYAQKFQGRITVTRDTSAATVYMELSNLTSEDTAVYFCS RGVSFWGQGTLVTVSSASTKG 127 8ANC65HC QVQMVASGGGLVKPGGSLRLSCEASGFTFSDYYMSWVRQAPGKGLEW ISYITSGGNALYYADSVKGRFTISRDNAKNSLYLQMNSLRAEDTAVYYCA RDLLHAHDFGRQGTLVTVSSASTKG 128 8ANC67HC QVQLVESGGGVVQPGRSLRLSCATSGFTSKNYGVHWVRQAPGKGLEW VAVIWYDGSNKFYADSVKGRFTISRDRSKNMVYLQMNSLRVEDTAIYYC ARDSVAFVLEGPIDYWGQGTLVTVSSASTKG 129 8ANC69HC QVQLVQSGAEVKKPGASVKVSCKASGYTFTDYYIHWVRQAPGQGLEW MGWINPSTGGTNFVQKFLGRVTMTSDTSINTAYMELRRLKNDDAAIYYC ATYSTRQFFHYYYVTDVWGQGTTVTVSSASTKG 130 8ANC6HC QVQLVQSGAEVKKPGSSVKVSCRASGGSFGNYAINWVRQAPMQGLEW MGGIIPIFGTTNYAQNFRGRVTINADTFTNTVNMDLSSLRSEDTAVYYCG RSINAAVPGLEGVYYYYGMAVWGQGTTVTVSSASTKG 131 8ANC70HC QVQLHQWGAGLLKPSDTLSLTCGILGVSPPGSLTGYYWTWIRQPPGKG LEWIGEVYHSGSTNYNPSLASRVTISMGTTKTQFSLRLTSVTAADSAVYY CASGKVWGITARPRDAGLDVWGQGTTVTVTSASTKG 132 8ANC71HC EVQVVESGGGLVQPGGSLRLSCVASGFTFSEYWMSWVRQAPGKGLEW VATIKRDGSEESYVDSVKGRFTISRDNAKNSLYLQMNSLRAEDTAVYYC ARVRDPNYNLHFDSWGQGTLVTVSSASTKG 133 8ANC72HC QVQLVESGGGLIQPGGSLRLSCEASGFAVGDINYMSWVRQAPGKGLEW VSVLYSGGSSQYADSVKGRFTISRDNSRNTLYLQMDNLRAEDTAVYYCA RGLRVYFDLWGQGILVTVSSASTKG 134 8ANC74HC QVQLVQSGAEVKKPGSSVKVSCKASGGTFSTYAFSWVRQAPGQGLEW MGGIIPIFGTENYAQKFQGRVTITADKSTSTAYMELSSLRSEDTAVYYCA RDRSSAIGYCSSISCYKGSFDIWGQGTMVTVSSASTKG 135 8ANC75HC QVQLQESGPGLVKPSETLSLTCTVSGGSISSRSYYWGWIRQPPGKGLE WVGSIYYTGSTYYSPSLKSRVTISVDTSQNQFSLKLNSVTAADTAVYYCA RQKGSGTSLLYWGQGTLVTVSSASTKG 136 8ANC76HC QVQLVQSGSELKKPGASVKVSCKASGYTFTSYAINWVRQAPGQGLEWM GWINTNTGNPTYAQGFTGRFVFSLETSVSTAYLQINSLKAEDTAVYYCAR DLLESRTYYNDIRDCWGQGTLVTVSSASTKG 137 8ANC78HC QVQLQESGSGLVKPSGTLSLTCAVSNGPISSGNWWSWVRQTPEKGLE WIGEVYHSGSTNHNPSLKSRATILVDKSKNQFSLNLRSVTAADTAVYYCA RVRGSWNFDYWGQGILVTVSSASTKG 138 8ANC79HC QHQLVPCVAEVRKPGASVKVSCKVSGYTLTEISMHWVRQAPGKGLEW MGGFDREDGETIYAQKFQGRVTMTEDTSTDTAYMELSSLRSEDTAVYY CATTYLAVVPDGFDGYSSSWYWFDPWGQGTLVTVSSASMQGPMLLSP TGTLLPRAPLVQTRPGP 139 8ANC7HC QVQLVQSGAEVRKPGSSLKVSCKSSGGTFSRYVVNWVRQAPGQGLEW MGGIIPIFGIAKYAQKFQDRVTMTADESKNTVYLDFSSLRSDDTAVYYCA RDRGDTRLLDYGDYEDERYYYGMDVWGQGTTVIVSSASTKG 140 8ANC80HC QVQLVQSGAEVKKPGSSVKVSCKASGGTFSTYAFSWVRQAPGQGLEW MGGIIPIFGTENYAQKFQGRVTITADKSTSTAYMELSSLRSEDTAVYYCA RDRSSAIGYCSSISCYKGSFDIWGQGTMVTVSSASTKG 141 8ANC82HC QVHLEESGPGLVKTSQTLSLTCSVSSYSISRSGYFWTWIRQRPGKGLEW IGYIYFNGRTTYNPSLKSRITISRDTSHSQFSLTLNSLSAADTAVYYCGRC QDGLASRPIDFWGQGTLVTVSSASTKG 142 8ANC83HC QVQLVESGGGVVQPGKSLRLSCAISGFLFNNYGGQWVRQAPGKGLEW VAAISYDGNNRYYADSAKGRFLISRDTPKNILYLQIYSLRLDDTAVYYCAR DSVSKSYSAPPEFWGQGTVVTVSSASTKG 143 8ANC91HC QLQLQESGPGLVKPSETLSLTCSVSDGSINSNSYYWAWIRQSPGKGLE WIGSVYYFGGTYYSPSLKSRVTMSVDRSKNQFSLNVSSVTAADTAIYYC ARHVRPYDRSGYPERPNWFDPWGRGTLVTVSSASTKG 144 8ANC92HC RVQLVQSGAEVKKPGSSVTVSCKASGGSFSSYAISWVRQAPGQGLEW VGGVKVMFGTVHYSQKVQGRVTITADDSTGTSYLELSGLRSADTAVYYC ARNAGAYFYPFDIWGQGTLIIVSSASTKG 145 8ANC93HC QVQLVQSGAEVKKPGASVKVSCKASGYTFTRYHIHWVRHAPGQGLEW MGKINPSRASTKYAKKFQDRVTMTRDTSTSTVYMELSSLRGDDTAVYYC GREMGTFTLLGVVIDHYDFYPMDVWGQGTPVTVSSASTKG 146 8ANC9HC QVQLVQSGAEVRKPGSSLKVSCKSSGGTFSRYVVNWVRQAPGQGLEW MGGIIPIFGIAKYAQKFQDRVTMTADESKNTVYLDFSSLRSGDTAVYYCA RDRGDTRLLDYGDYEDERYYYGMDVWGQGTTVTVSSASTKG 147 12A10HC SQHLVQSGTQVKKPGASVRVSCQASGYTFTNYILHWWRQAPGQGLEW MGLIKPVFGAVNYARQFQGRIQLTRDIYREIAFLDLSGLRSDDTAVYYCA RDESGDDLKWHLHPWGQGTQVIVSPASTKG 148 12A12HC SQQLVQSGTQVKKPGASVRISCQASGYSFTDYVLHWWRQAPGQGLEW MGWIKPVYGARNYARRFQGRINFDRDIYREIAFMDLSGLRSDDTALYFC ARDGSGDDTSWHLDPWGQGTLVIVSAASTKG 149 12A13HC SQQLVQSGTQVKKPGASVRISCQASGYSFTDYVLHWYRQAPGQGLEW MGWIKPVYGARNYARRFQGRINFDRDIYREIAFMDLSGLRSDDTALYFC ARDGSGDDTSWYLDPWGQGTLVIVSAASTKG 150 12A16HC SQQLVQSGTQVKKPGASVRISCQASGYTFTDYVLHWWRQAPGQGLEW MGWIKPVYGARNYARRFQGRINFDRDIYREIAYMDLSGLRSDDTARYFC ARDGSGDDTSWHLHPWGQGTLVIVSAASTKG 151 12A17HC SQQLVQSGTQVKKPGASVRVSCQASGYTFMNYIIHWWRQAPGQRLEW MGWINPVFGARNYAHRFQGRINFDRDINRETFQMELTGLRSDDTAVYYC ARDGSGDARDWHLDPWGQGTLVIVSSASTKG 152 12A1HC SQHLVQSGTQVKKPGASVRVSCQASGYTFTNYILHWWRQAPGQGLEW MGLIKPVFGAVNYARQFQGRIQLTRDINREIAFLDLSGLRSDDTAVYYCA RDESGDDLKWHLHPWGQGTQVIVSPASTKG 153 12A20HC SQQLVQSGTQVKKPGASVRVSCQASGYTFMNYIIHWWRQAPGQRLEW MGWINPVFGARNYAHRFQGRINFDRDINRETFQMDLTGLRSDDTAVYYC ARDGSGDARDWHLHPWGQGTLVIVSSASTKG 154 12A21HC SQHLVQSGTQVKKPGASVRVSCQASGYTFTNYILHWWRQAPGQGLEW MGLIKPVFGAVNYARQFQGRIQLTRDIYREIAFLDLSGLRSDDTAVYYCA RDESGDDLKWHLHPWGQGTQVIVSPASTKG 155 12A22HC SQQLVQSGTQVKKTGASVRVSCQASGYDFTKYLIHWWRQAPGQGLEW MGWMKPVYGATNYAHRFQGRISFTRDIYREIAFMDLNGLRSDDTAVYFC ARDGGGDDRTWLLDAWGQGTLVIVSSASTKG 156 12A23HC SQHLVQSGTQVKKPGASVRVSCQASGYTFTNYILHWWRQAPGQGLEW MGLIKPVFGAVNYARQFQGRIQLTRDINREIAFLDLSGLRSDDTAVYYCA RDESGDDLKWHLHPWGQGTQVIVSPASTKG 157 12A27HC SQQLVQSGTQVKKPGASVRISCQASGYTFTDYVLHWWRQAPGQGLEW MGWIKPVYGARNYARRFQGRINFDRDIYREIAFLDLSGLRSDDTARYFCA RDGSGDDTSWHLHPWGQGTLVIVSAASTKG 158 12A2HC SQQLVQSGTQVKKPGASVRISCQASGYTFTDYVLHWWRQAPGQGLEW MGWIKPVYGARNYARRFQGRINFDRDIYREIAYMDLSGLRSDDTARYFC ARDGSGDDTSWHLHPWGQGTLVIVSAASTKG 159 12A30HC SQQLVQSGTQVKKPGASVRISCQASGYTFTDYVLHWWRQAPGQGLEW MGWIKPVYGARNYARRFQGRINFDRDIYREIAYMDLSGLRSDDTARYFC ARDGSGDDTSWHLHPWGQGTLVIVSAASTKG 160 12A37HC SQQLVQSGTQVKKTGASVRVSCQASGYDFTKYLIHWWRQAPGQGLEW MGWMKPVYGATNYAHRFQGRISFTRDIYREIAFMDLNGLRSDDTAVYFC ARDGGGDDRTWLLDAWGQGTLVIVSSASTKG 161 12A46HC SQQLVQSGAQVKKPGASVRVSCQASGYTFTNHFLHWWRQAPRQGLE WMGWINPVHGGRNYARRFQGRINFGRDVYQETAYMELSGLRNDDTAT YFCARGGGDGRNWHLHPWGQGTLVIVSAASTKG 162 12A4HC SQHLVQSGTQVKKPGASVRVSCQASGYTFTNYILHWWRQAPGQGLEW MGLIKPVFGAVNYARQFQGRIQLTRDIYREIAFLDLSGLRSDDTAVYYCA RDESGDDLKWHLHPWGQGTQVIVSPASTKG 163 12A55HC SQQLVQSGAQVKKPGASLRVSCQASGYTFMNYLLHWWRQAPGQGLE WMGWINPVYGAVNYAHRFQGRLTFSRDVYREIAYMDLNGLRSDDTAVY FCARDGSGDDRNWHLDPWGQGTLVIVSSASTKG 164 12A56HC SQQLVQSGTQVKKPGASVRVSCQASGYTFTNYILHWWRQAPGRGLEW MGLIKPVYGAVNYARQFQGRIQLTRDIYREIAFLDLSGLRPDDTAVYYCA RDESGYDLNWHLDSWGQGTQVIVSPASTKG 165 12A6HC SQQLVQSGTQVKKPGASVRVSCQASGYTFTDYVLHWWRQAPGQGLE WMGWIKPVYGARNYAHRFQGRINFDRDVYREIAYMDLSGLRSDDTAVY FCARDGSGDATSWHLHPWGQGTLVIVSSASTKG 166 12A7HC SQQLVQSGTQVKKPGASVRVSCQASGYTFMNYIIHWWRQAPGQRLEW MGWINPVFGARNYAHRFQGRINFDRDINRETFQMELTGLRSDDTAVYYC ARDGSGDARDWHLDPWGQGTLVIVSSASTKG 167 12A9HC QVTLVQSGAEVKKPGASVRISCRASGFTFDDYSDYSFIPTTYLIHWFRQA PGQGLEWMAWINSVNGGRNIARQFQGRVTVARDRSNSIAFLEFSGLRH DDTAVYFCARDRRDDDRAWLLDPWGQGTRVTVSSASTKG 168 LSSB2339HC QVRLEQSGAAMRKPGASVTLSCQASGYNFVKYIVHWVRQKPGLGFEW VGMIDPYRGRPWSAHKFQGRLSLSRDTSMEILYMTLTSLTSDDTATYFC ARAEAASDSHSRPIMFDHWGQGSRVTVSSASTKG 169 LSSB2351HC QVRLEQSGTAVRKPGASVTISCQASGYNFVKFFIHWVRQRPGQGFEWV GMIEPFRGRPWSAGNFQGRLSLSRDVSTETLYMTLNNLRSDDTAVYFC ARLEAESDSHSRPIMFDHWGHGSLVTVSSASTKG 170 LSSB2361HC QVRLFQSGAAMRKPGASVTISCEASGYNFMNYFVHWVRQRPGRGFEW LGMINPRGGRPWSAQSVQGRLTLTRDTSTEMFYMRLDGLRSDDTATYF CARNEADYHDGNGHSLRGMFDYWGQGSLITVSSASTKG 171 LSSB2364HC QVRLEQSGAAVRKPGASVTLSCQASGYNFVNYIIHWVRQRPGLDFEWV GMIDPYRGRPWSAHKFQGRLSLSRDVSTEILYMTLSSLRSDDTATYFCA RAEAESQSHSRPIMFDFWGQGSRVTVSSASTKG 172 LSSB2367HC QVRLSQSGAAIKKPGASVTISCETEGYTFINYIIHWVRQPPGRGFEWLGM IDPRNGRPWFGQSVQGRLSLRRDTYTEVVYMTLSGLTSDDAGHYFCAR NEPQYHDGNGHSLPGMFDYWGQGTLVAVSSASTKG 173 LSSB2416HC QVRLSQSGAAVKKPGASVTIVCETEGYNFIDYIIHWVRQPPGRGFEWLG MIDPRNGRPWSGQKVHGRLSLWRDTSTEKVYMTLTGLTSDDTGLYFCG RNEPQYHDDNGHSLPGMIDYWGQGTMVTVSSASTKG 174 LSSB2434HC QVRLFQSGAAMRKPGASVTISCEASGYNFMNYFVHWVRQRPGRGFEW LGMINPRGGRPWSAQSVQGRLTLTRDTSTEMFYMRLDGLRSDDTATYF CARNEADYHDGNGHSLRGMFDYWGQGSLITVSSASTKG 175 LSSB2483HC QVRLFQSGAAMRKPGASVTISCEASGYNFMNYFVHWVRQRPGRGFEW LGMINPRGGRPWSAQSVQGRLTLTRDTSTEMFYMRLDGLRSDDTATYF CARNEADYHDGNGHSLRGMFDYWGQGSLITVSSASTKG 176 LSSB2490HC QVRLFQSGAAMRKPGASVTISCEASGYNFMNYFVHWVRQRPGRGFEW LGMINPRGGRPWSAQSVQGRLTLTRDTSTEMFYMRLDGLRSDDTATYF CARNEADYHDGNGHSLRGMFDYWGQGSLITVSSASTKG 177 LSSB2503HC QVRLEQSGAAVRKPGASVTLSCQASGYNFVRYIIHWVRQRPGLDFEWV GMIDPYRGRPWSAHKFGGRLSLTRDVSTEILYMTLTSLRSDDTATYFCA RAEAESQSHSRPIMFDSWGQGSRVTVSSASTKG 178 LSSB2525HC QVRLEQSGNAVRKPGASVTISCQASGYNFVKFFIHWVRQRPGQGFEWV GMIEPFRGRPWSAGNFQGRLSLSRDVSTETLYMTLNNLRSDDTAVYFC ARLEAESDSHSRPIMFDHWGHGSLVTVSSASTKG 179 LSSB2530HC QVRLEQSGAAMRKPGASVTLSCQASGYNFVKYIIHWVRQKPGLGFEWV GMIDPYRGRPWSAHKFQGRLSLSRDTSMEILYMTLTSLKSDDTATYFCA RAEAASDSHSRPIMFDHWGQGSRVTVSSASTKG 180 LSSB2538HC QVRLFQSGAAMRKPGASVTISCEASGYNFLNYFVHWVRQRPGRGFEWL GMINPRGGRPWSAQSVQGRLTLTRDTSTEMFYMRLDGLRSDDTATYFC ARNEADYHDGNGHSLRGMFDYWGQGSLITVSSASTKG 181 LSSB2554HC QVRLEQSGAAMRKPGASVTLSCQASGYNFVKYIIHWVRQKPGLGFEWV GMIDPYRGRPWSAHKFQGRLSLSRDTSMEILYMTLTSLKSDDTATYFCA RAEAASDSHSRPIMFDHWGQGSRVTVSSASTKG 182 LSSB2573HC QVRLSQSGAAIKKPGASVTISCETEGYTFINYIIHWVRQPPGRGFEWLGM IDPRNGRPWFGQSVQGRLSLRRDTYTEVVYMTLSGLTSDDTGLYFCAR NEPQYHDGNGHSLPGMFDSWGQGTLVAVSSASTKG 183 LSSB2578HC QVQLFQSGAAMRKPGASVTISCEASGYNFMNYFVHWVRQRPGRGFEW LGMINPRGGRPWSAQSVQGRLTLTRDTSTEMFYMRLDGLRSDDTATYF CARNEADYHDGNGHSLRGMFDYWGQGSLITVSSASTKG 184 LSSB2586HC QVRLEQSGAAMRKPGASVTLSCQASGYNFVKYIVHWVRQKPGLGFEW VGMIDPYRGRPWSAHKFQGRLSLSRDTSMEILYMTLTSLKSDDTATYFC ARAEAASDSHSRPIMFDHWGQGSRVTVSSASTKG 185 LSSB2609HC QVRLFQSGAAMKKPGASVTISCEASGYNFMNYFVHWVRQRPGRGFEW LGMINPRGGRPWSAQSVQGRLTLTRDISTEMFYMRLDGLRSDDTATYF CARNEADYHDGNGHSLRGMFDYWGQGSLITVSSASTKG 186 LSSB2612HC QVRLEQSGTAMRKPGASVTLSCQASGYNFVKYIVHWVRQKPGLGFEWV GMIDPYRGRPWSAHKFQGRLSLSRDTSMEILYMTLTSLKSDDTATYFCA RAEAASDSHSRPIMFDHWGQGSRVTVSSASTKG 187 LSSB2630HC QVRLFQSGAAMRKPGASVTISCEASGYNFMNYFVHWVRQRPGRGFEW LGMINPRGGRPWSAQSVQGRLTLTRDTSTEMFYMRLDGLRSDDTATYF CARNEADYHDGNGHSLRGMFDYWGQGSLITVSSASTKG 188 LSSB2640HC QVRLFQSGAAMRKPGASVTISCEASGYNFMNYFVHWVRQRPGRGFEW LGMINPRGGRPWSAQSVQGRLTLTRDTSTEMFYMRLDGLRSDDTATYF CARNEADYHDGNGHSLRGMFDYWGQGSLITVSSASTKG 189 LSSB2644HC QVRLSQSGAAIKKPGASVTISCETEGYTFINYIIHWVRQPPGRGFEWLGM IDPRNGRPWFGQSVQGRLSLRRDTYTEVVYMTLSGLTSDDTGLYFCAR NEPQYHDGNGHSLPGMFDSWGQGTLVAVSSASTKG 190 LSSB2665HC QVRLFQSGAAMRKPGASVTISCEASGYNFMNYFVHWVRQRPGRGFEW LGMINPRGGRPWSAQSVQGRLTLTRDTSTEMFYMRLDGLRSDDTATYF CARNEADYHDGNGHSLRGMFDYWGQGSLITVSSASTKG 191 LSSB2666HC QVRLEQSGAAMRKPGASVTLSCQASGYNFVKYIIHWVRQKPGLGFEVW GMIDPYRGRPWSAHKFQGRLSLSRDTSMEILYMTLTSLKSDDTATYFCA RAEAASDSHSRPIMFDHWGQGSRVTVSSASTKG 192 LSSB2669HC QVRLEQSGAAMRKPGASVTLSCQASGYNFVKYIIHWVRQKPGLGFEWV GMIDPYRGRPWSAHKFQGRLSLSRDTSMEILYMTLTSLKSDDTATYFCA RAEAASDSHSRPIMFDHWGQGSRVTVSSASTKG 193 LSSB2680HC QVRLEQSGVAMRKPGASVTLSCQASGYNFVKYIIHWVRQKPGLGFEWV GMIDPYRGRPWSAHKFQGRLSLSRDTSMEILYMTLTSLKSDDTATYFCA RAEAASDIHSRPIILTGPGEYGLDLEHMDWTWRILCLLAVAPGCHSQ 194 LSSB2683HC QVRLEQSGAAMRKPGASVTLSCQASGYNFVKYIVHWVRQKPGLGFEW VGMIDPYRGRPWSAHKFQGRLSLSRDTSMEILYMTLTSLKSDDTATYFC ARAEAASDSHSRPIMFDHWGQGSRVTVSSASTKG 195 LSSB344HC QVRLEQSGTAVRKPGASVTISCQASGYNFVKFFIHGVRQRPGQGFEWV GMIEPFRGRPWSAGNFQGRLSLSRDVSTETLYMTLNNLRSDDTAVYFC ARLEAESDSHSRPIMFDHWGHGSLVTVSSASTKG 196 LSSNEC107HC QVRLVQSGPQVKTAGASMRVSCEASGYRFLDYIIVWIRQTHGQHFEYVG MINPRGGTPWPSSKFRDRLTLTRDIYTDTFYLGLNNLGSGDTAIYFCARL EADGDDYSPKMFDYWGQGTRIIVSAASTKG 197 LSSNEC108HC QVHTFQSGSSMKKSGASVTISCEATGYNIKNYILHWVRQKPGRGFEWV GMIDPINGRPWFGQPFRGRLTLTRDLSTETFYMSLSGLTSDDTATYFCA RREADYHDGNGHTLPGMFDFWGPGTLITVSSASTKG 198 LSSNEC109HC QVSLVQSGPQVKTPGASMRVSCETSGYRFLDYIIVWIRQTHGQHFEYVG MINPRGGTPWPSSKFRDRLTMTRDIHTDTFYLGLNNLRSDDTAIYFCARL EADGDDYSPKMFDYWGQGTRIIVSAASTKG 199 LSSNEC110HC QVRLVQSGPQMKTPGASLRLSCEVSGYRFLDYFIVWVRQTGGQGFEYV GMINPRGGRPWSSWKFRDRLSLTRDIETDTFYLGLNNLRSDDTAIYFCA RLEADGDNYSPKMVDYWGQGTKIIVSPASTKG 200 LSSNEC116HC QVRLSQSGAAVVKTGASVTISCETEGYNFVNYIIHWVRRPPGRGFEWLG MIDPRNGHPWFAQTVRGRLSLRRDTFKETVYMTLSGLTSDDTGVYFCA RNEPQYHSLPGMFDYWGHGTPVTVSSASTKG 201 LSSNEC117HC QVRLVQSGAQLKKPGASVTVSCEASGYNFVNYIINWVRQTPGRGFEWV GMIDPRRGRPWSAQKFQGRLTLTRDIDSEKLYMHLSGLRGDDTAVYYC ARQDSDFHDGHGHTLRGMFDSWGQGSPVTVSSASTKG 202 LSSNEC118HC QVRLVQSGPQVKTPGASMRISCEASGYRFQDYIIVWIRQTHGQGFEYVG MINPRGGTPWSSSKFRDRLSLTRDIYTDTFYLGLNNLGSDDTAIYFCARL EADGGDYSPKMFDYWGQGTRIIVSAASTKG 203 LSSNEC11HC QVRLFQSGAAMRKPGASVTISCEASGYNFMNYFVHWVRQRPGRGFEW LGMINPRGGRPWSAQSVQGRLTLTRDTSTEMFYMRLDGLRSDDTATYF CARNEADYHDGNGHSLRGMFDYWGQGSLITVSSASTKG 204 LSSNEC122HC QVRLVQSGPQVKRPGASIRLSCETSGYRFQDYIVAWIRQTRGQRFEFVG MVNPRGGRPWPSSKFRDRVTLTRDIESETFHLGLNDLTSDDTATYFCAR LEADGADYSPKMFDFWGQGTKIVVSPASTKG 205 LSSNEC123HC QVRLEQSGAAVRKPGASVTLSCQASGYNFVNYIIHWVRQRPGLDFEWV GMIDPYRGRPWSAHKFEGRLSLSRDVSTEVLYMTLSSLRSDDTATYFCA RAEAESQSHSRPIMFDYWGQGSRVTVSSASTKG 206 LSSNEC127HC QVRLEQSGAAMRKPGASVTLSCQASGYNFVKYIIHWVRQKPGLGFEWV GMIDPYRGRPWSAHKFQGRLSLSRDTSMEILYMTLTSLKSDDTATYFCA RAEAASDSHSRPIMFDHWGQGSRVTVSSASTKG 207 LSSNEC18HC QVRLSQSGAAVMKTGASVTISCETEGFNFVNYIIHWVRRPPGRGFEWLG MIDPRNGHPWFAQTVRGRLSLRRDTFNEIVYMTLSGLTTDDTGLYFCAR NEPQYHSLPGMFDYWGQGTPVTVSSASTKG 208 LSSNEC24HC QVRLSQSGAAMKKPGASVTISCETEGYTFINYIIHWVRQPPGRGFEWLG MIDPRNGRPWFGQSVQGRLSLRRDTYTEVVYMTLSGLTSDDAGLYFCA RNEPQYHDGNGHSLPGMFDYWGQGTLVAVSSASTKG 209 LSSNEC29HC QVRLSQSGAAVVKTGASVTISCETEGYTFVNYIIHWVRQSPGRGFEWLG MIDPRNGHPWFGQRLRGRLSLRRDRSTETVFMTLSGLTSDDTAIYFCAR NEPQYYDGSGHSLPGMFDYWGQGTRVWSSASTKG 210 LSSNEC2HC QVRLFQSGAAMRKPGASVTISCEASGYNFMNYFVHWVRQRPGRGFEW LGMINPRGGRPWSAQSVQGRLTLTRDTSTEMFYMRLDGLRSDDTATYF CARNEADYHDGNGHSLRGMFDYWGQGSLITVSSASTKG 211 LSSNEC33HC QVRLVQSGPQVKTPGASIRLSCEASGYRFLDYFIVWVRQTPGQGFEYVG MINPRGGRPWSSWKFRDRLSLTREIDTDTFYLGLSNLRSDDTAIYFCARL EADGDDYSPKMVDYWGQGTKIIVSAASTKG 212 LSSNEC34HC QVRLFQSGAAMRKPGASVTISCEASGYNFMNYFVHWVRQRPGRGFEW LGMINPRGGRPWSAQSVQGRLTLTRDTSTEMFYMRLDGLRSDDTATYF CARNEADYHDGNGHSLRGMFDYWGQGSLITVSSASTKG 213 LSSNEC3HC QVRLEQSGAAVRTPGASVTLSCQASGYKFVNYIIHWVRQRPGLAFEVV GMIDPYRGRPWSAHSFEGRLSLSRDVSMEILYMTLTSLRSDDTATYFCA RAEAESQSHSRPIISTSGAR 214 LSSNEC46HC QVQFFQSGSSMKKSGASVTISCEATGYNIKNHILHWVRQKPGRGFEWV GMIDPINGRPWFGQAFRGRLTLTRDLSTETFYMSLSGLTSDDTATYFCA RREADYHDGNGHTLPGMFDFWGPGTLVTVSSASTKG 215 LSSNEC48HC QVRLSQSGAAVVKTGASVTISCETEGYTFVNHIIHWVRQPPGRGFEWLG MIDPRNGHPWFGQRLRGRLSLRRDRSTETVFMTLSGLTSDDIGIYFCAR NEPQYFDGSGHSLPGMFDYWGQGTRVVVSSASTKG 216 LSSNEC52HC QVRLSQSGAAVVKTGASVTISCETEGYTFVNYIIHWVRQPPGRGFEWLG MIDPRNGHPWFGQRLQGRLSLRRDRSTETVFMTLSGLTSDDTGIYFCAR NEPQYYDGSGHSLPGMFDYWGQGTRVWSSASTKG 217 LSSNEC56HC QVRLVQSGPQVKTPGASMRVSCEASGYRFLDYIIVWIRQTHGQHFEYVG MINPRGGTPWPSSKFRDRLSLTRDIHTDTFYLGLNNLGSDDTAIYFCARL EADGDDYSPKMFDHWGQGTRIIVSAASTKG 218 LSSNEC60HC QVRLEQSGAAVKKPGASVTISCQASGYNFVKFFIHWVRQRPGQGFEWV GMIEPYRGRPWSAGNFQGRLSLSRDVSTETLYMTLNNLRSDDTAVYFC ARLEAESDSHSRPIMFDHWGHGSLVTVSSASTKG 219 LSSNEC66HC QVRLSQSGAAVMKTGASVTISCETEGYNFVNYIIHWVRRPPGRGFEWLG MIDPKNGHPWFAQAVRGRLSLRRDTFNEVVYMTLSGLTSDDTGLYFCA RNEPQYHDGNGHSLPGMFDFWGQGTLVTVSSASTKG 220 LSSNEC70HC QVRLSQSGAAVVKTGASVTISCETEGYTFVNYIIHWVRQPPGRGFEWLG MIDPRNGHPWFGQRFRGRLSLRRDRSTETVFMTLSGLTSDDNGIYFCA RNEPQYYDGSGHSLPGMFDYWGQGTRWVSSASTKG 221 LSSNEC72HC QVRLEQSGAAVRKPGASVTLSCQASGYNFVNYIIHWVRQRPGLDFEWV GMIDPYRGRPWSAHKFQGRLSLSRDVSTEILYMTLSSLRSDDTATYFCA RAEAESQSHSRPIMFDFWGQGSRVTVSSASTKG 222 LSSNEC7HC QVRLEQSGAAVRKPGASVTLSCQASGYNFVNYIIHWVRQRPGLDFEWV GMIDPYRGRPWSAHKFQGRLSLSRDVSTEILYMTLNSLRSDDTATYFCA RAEAESQSHSRPIMFDSWGQGSRVTVSSASTKG 223 LSSNEC82HC QVRLFQSGAAMRKPGASVTISCEASGYNFMNYFVHWVRQRPGRGFEW LGMINPRGGRPWSAQSVQGRLTLTRDTSTEMFYMRLDGLRSDDTATYF CARNEADYHDGNGHSLRGMFDYWGQGSLITVSSASTKG 224 LSSNEC89HC QVRLEQSGGALRKPGASVTLSCQASGYNFVKYIIHWVRQRPGLGFEWV GMIDPYRGRPWYAHSFAGRLSLSRDTSTETLYMTLSSLKSDDTATYFCA RAEAASDSHSRPIMDWTWRILCLLAVVPASTKG 225 LSSNEC8HC QVRLFQSGAAMRKPGASVTISCEASGYNFMNYFVHWVRQRPGRGFEW LGMINPRGGRPWSAQSVQGRLTLTRDTSTEMFYMRLDGLRSDDTATYF CARNEADYHDGNGHSLRGMFDYWGQGSLITVSSASTKG 226 LSSNEC94HC QVRLEQSGAAMRKPGASVTLSCQASGYNFVKYIVHWVRQKPGLGFEW VGMIDPYRGRPWSAHKFQGRLSLSRDTSMEILYMTLTSLKSDDTATYFC ARAEAASDSHSRPIMFDHWGQGSRVTVSSASTKG 227 LSSNEC95HC QVRLVQSGPQVKRPGASIRLSCESSGYRFQDYIVAWIRQTRGQGFEFVG MVNPRGGRPWPSSRFRDRVTLTRDIESETFYLGLNDLTSDDTATYFCAR LEADGSDYSPKMFDFWGQGTKIVVSPASTKG 228 LSSNEC9HC QVRLVQSGAQLKKPGASVTVSCEASGYNFVNYIINWVRQTPGRSFEWV GMIDPRRGRPWSAQKFQGRLTLTRDIDSEKLYMHLSGLRGDDTAVYYC ARQDSDFHDGHGHTLRGMFDSWGQGSPVTVSSASTKG 229 LSSB2055HC QVQLVQSGPELMKPGSSVKVSCRASGDNFLTSTFNWLRQAPGQRLEW MGRFIPSLGLITSAPKFSDRLTITADQATLTAYMELTGLTSEDTALYYCAR GLCRGGNCRLGPSGWLDPWGRGTQVTVSSASTKG 230 LSSB2066HC QWLIQSGAEVKRPGSSVKVSCKASGGSFPITWVRQAPGHGLEWMGGI NPFFGTTNYAQKFQGRVSITADESTSTTYLHLSDLRSEDTAVYFCARENR EKWLVLRSWFAPWGQGTLVTVSSASTKG 231 LSSB2068HC EESGPGLVKPSQTLSLTCSVSGDSVSSGGYFWSWIRQHPTKGLECLGY VYYTGNTYYNPSLKSPPTIEVAMANNQVSLKLGSVTAADTAVYYCARIKR FRGGNYFDTWGHGLLVTVSSASTKG 232 LSSB2080HC LAQLEQSGGGVVKPGGSLRLPCAASGFTFIDYYMAWIRLAPGKGLEWLS YISKNGDYTKYSESLKGRFTISRDNAKNLVILQLNRLRADDTAIYFCARAD GLTYFGELLQYIFDLWGQGARVIVSSASTKGPSVFPLAPSSKSTSGHASV 233 LSSB2133HC QVQLVQSGAEVKKPGASVKISCKASGYSFRNYAVHWVRQAPGQGLEW MGEINGGNGNTEYSQKSQGRLTITRDISATTAYMELSSLRSDDTAVYYC ARVAYVHVVTTRSLDNWGQGTLVTVSSASTKG 234 LSSB2182HC QVQIRQSGPGLVKPLETLSLSCIVFGGSFIAYHWTWIRQAPLKGLEWIGDI DQGGDITYSPSLKSRVTMSVDRSKSQFSLKLSSVTAADAAVYYCVRGPP NRYAVTSFTSGTHRERSSYYFDYWGPGTLVTVSSASTKG 235 LSSB218HC KAPATLSLSPGERATLSCRASQSVGSDLAWYQQKPGQAPRLLIYDASNR ATAIPARFSGSGSGTDFTLSISSLEPEDFAVYFCQQRYDKITFGQGTRLEI QRTVAAPSVFIFPPSDEQ 236 LSSB2277HC FVQLVESGGGVVQPGTSLRLSCTTSGFIFSDYGMHWVRQAAGKGLEWV AVIWHDGSNRFYADSVKGRFTISRDNSKNAVYLEMNNLRVEDTALYYCA RTSMDIDYWGQGTPVTVSSASTKG 237 LSSB2288HC QVYLVQSGPELKKPGASVKISCKASGYNFPKYAIHWVRQAPGQGLQWM GWINGDNGDARYSQKLQGRVTPSTDTSASVVYMELKRLRSEDTAVYYC ARALYPWEIGGVPSTMGDDYWGQGTLITVSSASTKG 238 LSSB331HC QVHLQQWGAGLLKPSETLSLTCAVSGGSFSGFFWTWIRQSPGKGLEWI GEVNHSGFTHSNPSLESRATISVAASNTQFSLRLASVTAADTAIYFCALR YFDWSPFRRDTYGTDVWGQGTTVIVSSASTKG 239 LSSNEC101HC QVQLVQSGAELKKPGSSVKVSCKASGGTFNNHTFNWVRQAPGQGLEW MGRTIPILGSRDYAKTFQDRVTIIADKSTSTVYLELRRLKSEDTGVYYCAT SMYYFDSGGYYRNTDLDKWGQGSLVTVSSASTKG 240 LSSNEC106HC GLDLEHDGHHKEEPRASVTVSCEASGYNFVNYIIHWVRLTPGRGFEWM GMIDPRRGRPWSAQKFQGRLTLTRDIDSERLYMQLSGLRGDDTAVYFC ARQEPDFHDGHGHTLRGMFDSWGQGSPVSVSSASTKG 241 LSSNEC112HC QVQLVQSGAELKKPGSSVKVSCKASGGTFSNYAINWVRQAPGQGFEW MGGIIPLFATPTYAQKFQGRVRITADDSTSTAYMELSSLRSDDTAVYFCA RPNVVRSALDYWGQGTLVTVSSASTKG 242 LSSNEC115HC QARLDQWGTGLLKPSETLSLKCAVFGVLFTDYNWTWVRQSPGKGLEWI GHLDHRGGGNYNPSLESRVTISLDYSKAQFSLHLKSVTVADTALYYCAG AVKGFWFDEVYNWFGPWSQGTLVTVASASTKG 243 LSSNEC124HC QVQLQESGPGLVKPSGTLSLTCAVSGASISSRNWWTWVRQPPGKGLE WIGEIYESGATNYNPSLKSRVTISVDKSKNQFSLRLTSVTAADTAVYFCA RLMTFGGLIGTLDYWGQGTLVTVLQPPPRAHRYHPRNLLQEHLCARVM P 244 LSSNEC125HC QVQLVQSGAEVKKPGSSVKVSCKASGGTFSTYAISWVRQAPGQGLEW MGGIIPSFSMSNYAQDFQGRLTITADESTSSVYMELNSLRSEDTAVYYCA RDFPRFHRLVGNYDFWRGTLDRFSYMDLWGRGTAVTVSSASTKG 245 LSSNEC126HC QVHLVQSGAEAKRPGSSVRVSCRASGGDFSSYTLSWVRQAPGQGIEW MGGWPMLDTVHYAQKFQGRLTLSVDEGTSTAYMELSSLRSEDTAMYY CTRGRQTFRAIWSGPPAVFDIWGQGTLVIVSSASTKG 246 LSSNEC14HC NGGSLRLSCRVSGFGFHLYEMNWVRQAPGKGLEWISSISGSGESTHYS DSITGRFSMSRDEAKDSLYLQMNNLRVEDTAVYYCTRGFSMGDGTGFS FDTWGRGTMVTVSSGLDTVSLASTKGPSVFPLAPCSRSTSDARLS 247 LSSNEC16HC AARLDQWGTGLVKPSETLSLKCAVFGVDFPDYTWTWARQAPGKGLEWI GHRDHRGGSSYNPSLSGRATISLDTSKAQFSLHIKSVTVADTATYYCAG AVAGLWFEDAYNWFGPWSQGTLVTVAAASTKGPSVFPLAPSSKSTSGH ASVL 248 LSSNEC21HC QARLDQWGTGLLKPSETLSLKCAVFGVLFTDYNWTWVRQSPGKGLEWI GHLDHRGGGNYNPSLESRVTISLDYSKAQFSLHLKSVTVADTALYYCAG AVKGLWFDETYTWFGPWSQGTRVTVASASTKGPSVFPLAPSSKSTSGT RDLS 249 LSSNEC30HC QVQLVQSEAEVKKPGSSVKVSCKASGGTFRGYTISWVRQAPGQGLEW MGRIIPILGKAIYAPSFQGRVTLTADKSTGTAYMELSRLRSDDTAVYYCAK VKMRGSSGYYYLFDDWGQGTLVTVSSASTKG 250 LSSNEC49HC QVHLVQSGAEVKKPGASVKVSCKVSGYTLSELSIHWVRQGPGRGLEW MANFDPEDGETIYAPQFQGRVTLTEDTSTDTAYMQLTSLRSEDTAVYYC ATDRYTDTGRWGPGTLVTVSSASTKG 251 LSSNEC54HC QARLDQWGTGLLKPSETLSLKCAVFGVLFTDYNWTWVRQSPGKGLEWI GHLDHRGGGSYNPSLESRVSISLDYSKAQFSLHLKSVTVADTALYYCAG AVKGFWFDEPSTWFGPWSQGTMVTVASASTKG 252 LSSNEC55HC QARLDQWGTGLLKPSETLSLKCAVFGVLFTDYNWTWVRQSPGKGLEWI GHLDHRGGGNYNPSLESRVTISLDYSKAQFSLHLKSVTVADTALYYCAG AVKGFWFDEVYNWFGPGVREPWLPSPQPPPRAHRSSPWHPPPRAPLV TATVP 253 LSSNEC57HC QARLDQWGTGLLKPSETLSLKCAVFGVLFTDYNWTWVRQSPGKELEWI GHLDHRGGGNYNPSLESRVTISLDYSKAQFSLHLKSVTVADTARYYCAG AVKGFWFDDPYTWFGPWSQGTLVTVASASTKG 254 LSSNEC5HC QVHLVQSGAEAKRPGSSVRVSCRASGGDFSSYTLSWVRQAPGQGLER MGGWPMLDTVHYAQKFQGRLTLSVDEGTSTAYMELSSLRSEDTAMYY CTRGRQTFRAIWSGPPWFDIWGQGTLVSVSSASTKG 255 LSSNEC67HC QFRLVQSGPEVKNPGSSVTVSCKASGGTFSGLGINWVRQAPGQGLEWL GDIKTMYGTTNYAPKFQGRVTITADESTSTSYMELSGLRSEDTAVFYCVR ELFGHHPAFGVWGQGTSVIVSSASTKG 256 LSSNEC74HC QVQLVQSGAEVKKPGASVKVSCKASGYTFTNYGVSWVRQAPGQGLEW MGWISPYSGNTNYAQRLQDRVTMTTDTSTNTAYMELRSLRSDDTAVYY CAARSYYYYSMDVWGQGTTVTVSSASTKG 257 LSSNEC77HC QVQLVQSGADVKKPGASVKVSCKVSGYTVSELSIHWVRQAPGKGLEW MGGFDPEDGKTVSAQNFQGRVTMTEDKSTGTANMELRSLRSEDTAVYY CATTVQLIVDFCNGGPCYNFDDWGQGTLVTVSSASTKG 258 LSSNEC85HC QVQLVQSGAEVKKPGSSVKVSCKASGGTLSSYTISWVRQAPGQGLEW MGRLIPLVDITTYAQKFQGRVTITADTSTNTAYMELSNLRSEDTAIYHCAT STMIAAVINDAFDLWGQGTTVTVSSASTKG 259 LSSNEC91HC QVQLVQSGAEVKKPGASVKVSCKASGNTFTSYGITWVRQAPGQGLEW MGWISAYNGNTNYAQKLQDRLTMTTDTSTSTAYMELRSLRSDDTAVYY CAFSRHYGSGNYDYWGQGTLVTVSSASTKG 260 LSSNEC92HC QVQLQQWGAGLLKPSETLSLTCAVYGGSFSGYYWSWIRQPPGKGLEWI GEINHSGSTNYNPSLKSRVTISVDTSKNQFSLKLSSVTAADTAVYYCARL PIGSGWYGRDYWGQGTLVTVSSASTKG 261 3A124HC EVQLLESGGGLVRPGGSLXLSCSASGFTFNSYAMSWVRQAPGKGLEW VSSVSASGEMTYYADSVRGRFTISRDNANNALHLQMNSLRAEXTAVYYC AKVGGTVWSGYSNYLDYWGPGTLVTVSSASTKG 262 3A125HC QVQLVQSGAEVKKPGASVKVSCKPSSNTFTSHYIHWVRQAPGQGLEW MGMINPGGSTRYAPKFQGRVTLTRDTSTRTVYMELSSLRSEDTAVYYCA RPQYNLGRDPLDVWGLGTMVTVSSASTKG 263 3A140HC EVQLVESGGGLVKPGGSLRLSCADSGFTFRSYSMHWVRQAPGKGLAW VSSISSTSNYIYYADSVKGRFTISRDNAKNSLYLQMNSLRAEDTAVYYCA RTFITASWFDSWGQGTLVTVSSASTKG 264 3A144HC VSGGRFSNYGLSWVRQAPGQGLEWMGRIVPAINRAKYAQKFQGRVILT ADKITDTAYMELRSLRSEDTAIFYCARDPQIEIRGNAFDIWGQGTWTVSS ASTKG 265 3A160HC QVQLQESGPGLVKPSGTLSLTCNVYGGSMISYYWSWIRQPPGKGLEWI GHVYNSGNTKYSPSLKNRVTISMDTSRNLFSLKVTSVTPADTAVYYCAR ADYDNIWDSRGGFDLWGQGTLVTVSSASTKG 266 3A18HC QVQLVQLLQSGAEVKKPGSSVKVSCQISGYGFSNYAISWVRQAPGQGL EWLGRIVPAVGMTEYAQKFQGRVTFTADRSTITAYMDLRGLRSDDTAVY YCVRDPQVEVRGNAFDIWGQGTMVTVSSASTKG 267 3A204HC QVQLVQSGAEMKKPGASVKVSCKASGHTFTNYYMHWVRQAPGQGLE WMGMINPTGDSTRYAQRFQGRVTMTRDTSTRTVYMELSSLRSDDTAVY YCARAHHDFWRAPVDVWGKGTTVTVSSASTKG 268 3A228HC EVQLVQSGAEVKKPGESLRISCKTSGYNFNDDWIAWVRQRPDKGPEW MGIFYPGDSQATYSPSFQGHVTFSADTSISTAYLQWTSLKASDTAIYYCA RTRCFGANCFNFMDVWGKGTALTVTVSSASTKG 269 3A233HC QVQLQESGPGPVKPSETLSLTCTVSGGSMISYYWSWIRQPPGKGLEWI GYIFTNGRTTYSPSLRSRVTISLDTSTNHFSLRLKSVTAADTAIYYCARLD GEAFRYYLDLWGQGNLVTVSSASTKG 270 3A244HC IRSFYWHWIRQSPGKGLEWLGSVFDNGLTTHNPSLKSRLTISEDPSRNQI SLKLRSMTAADTAVYYCARGDYDILTSSYQFDYWGQGTLVAVSSASTKG 271 3A255HC QVQLQESGPGLVKPSETLSLTCTVFGASIRSFYWHWIRQSPGKGLEWLG SVFDNGLTTYNPSLKNRLSISEDPSRNQISLNLRSMTAADTAVYYCARAD YDLLTSSYHFDSWGQGTLVTVSSASTKG 272 3A296HC QVQLQESGPGLVKPSETLSLTCTVSGGSISYYYWSWIRQPPGKGLEWIG DIYYSGTTDYNPSLKSRVTISVDTSKNQFSLKLSSVTAADTAVYYCARRR GQRLLAYFDYWGQGSLVTVSSASTKG 273 3A334HC QVQLVQSGAEVKKPGASVKVSCKAPGYTFIGHYMHWIRQAPGQGLEW MGWINPNSGDTNYAQTFQGRVTMTRDTSISTAYMELTRLRSDDTAVYY CARDLRPMRGNWAMHVWGEGTTVTVSSASTKG 274 3A366HC CTVSGGSISSAGYYWTWIRQHPGKGLEFIGYIYYIGTTYYNPSLKSRLTISI DTSKNQFSLKLSSVTAADTAIYYCARDYTARGRHFFDYWGQGALVTVSS ASTKG 275 3A381HC SSFAISWVRQAPGQGLEWMGGIIPIFEATSYAQKFQDRLTITTDESTTTAY MDLSSLRSEDTAVYYCARAQGDILTEGYFDYWGQGTLVTVSSASTKG 276 3A384HC QVQLVQSGAEVKKPGSSVKVSCKVSFFSNYGISWVRQRPGQGLEWMG RIIPAIDDMTYAQTFRGRVTFSADKFTTTAYMELTGLTFEDTATYFCARDP QVNRRGNCFDHWGQGTLVTVSSASTKG 277 3A419HC LEWMGRIIPAIDDVTYAQTFRGRVTFSADKFTTTAYMDLTGLRSEDTATY FCARDPQVNRRGNCFDHWGQGTLVTVSSASTKG 278 3A461HC QVQLVQSGAEVKKPGAAVKISCKASRFTFSSYYIHWVRQAPGQGLEWM GIINPSGGSTSNAQKFQDRVTLTRDMSTGTVYMELSRLTSEDTAVYYCA TPEPSSIVAPLYYWGQGTLVTVSSASTKG 279 3A474HC EVQLLESGGGLVQPGGSLRLSCAVSGFTFGGHAVSWVRQAPGKGLEW LSQISGTGSRTDYADAVKGRFTVSRDNSKKTVYLQMNSLRVEDTALFYC ATRSPGGGYAFDIWGQGAMVTVSSASTKG 280 3A518HC QVQLQESGPGLVKPSETLSLTCTVSGGSISSAGYYWSWIRQHPEKGLEF IGYIYYLGTTYYNPSLKSRVSISIDTSNNQFSLELSSVSAADTAIYYCARDY TASGRHFFDYWGQGTLVTVSSASTKG 281 3A539HC EVQLLESGGALVQPGGSLRLSCAASGFTFSTSSMSWVRQAPGKGLEWV SAIGSGRGSTFYADSVKGRFTISRDNSKNTLSLQMNSLTAEDTATYYCTK TGGLLRFPEVWGKGTTVTVSSASTKG 282 3A576HC QVQLVQSGAEVKKPGSSVKVSCKASGGTFSNYAISWVRQAPGQGLEW MGGIIPIFEAASYAQKFQDRLTITTDESTTTAYMDLSSLRSEDTAIYYCARA QGDILTEGYFDYWGQGTLVTVSSASTKG 283 3A613HC QVQLQESGPGLVKPSETLSLTCTVSGGSISTYYWSWIRQPPGKGLEWIG YISYSGSTNYNPSLKSRVTISVDTSKNQFSLKLSSVTAADTAVYYCARHK SVLLWFRELDYWGQGTLVTVSSASTKG 284 3A64HC QVQLVQSGAEVKKPGSSVKVSCKTSGVRFSSNAISWVRQAPGQGLEW MGRTTPMLGGANHAPSFKGRVTISADESTRTVYMEMSSLRYEDTAVYY CASGRREGLNFLLDYWGQGTLVTVSSASTKG 285 3A650HC QVQLVQSGAEVRKPGASVKVSCKTSGYTFTNSYIHWVRQAPGQGLEW MGIINPPGGNTYYAQKFHGRVTLTRDTSTSTVYMELNSLRSEDTAVYFC ARPHSPTNIPSRPLDYWGQGTLVTVSSASTKG 286 3A67HC QVQLVQSGAEVKKPGASVKVSCKVSGYPLAELSVHWVRQVPGKGLEW VGGFDPEEGKTVYAQKFQGRVTMTEDRSTDTVYMELISLRYEDTAVYYC ATDNPVLQLGELSSSLDYWGQGTLVTVSSASTKG 287 3A779HC PSETLSLTCRVSGASISNFYWTWIRQPAGKGLEWIGRLYSSDKTNYNPS LNGRVTMSLDTSKNQFSLRLTSMTDADTAIYYCAREKGQWVTLPPYYFD SWGQGILVTVSSASTKG 288 3A816HC NTFTSHYVHWVRQAPGQGLEWMGMINPGGTTRYAPKFQDRVTLTRDT STRTVYMELRSLRSEDTAVYYCARPQYNLGREPLNVWGQGTMVTVSSA STKG 289 3A869HC QVQLQESGPGLVKPSETLSLTCSVSGASISNFYWTWIRQPAGKGLEVV GRLYSSDRTNYNPSLNGRVTMSLDTSKNQFSLRLTSMTDADTAIYFCAR EKGQWLTVPPYYFDSWGQGILVTVSSASTKG 290 3A93HC CTVSGGSHSYYWNWIRQSPGKGLEWLGYIFDGGRANYNPSLRSRLTMS VDTSKNQISLKVKSVTAADSAIYYCARLDGEAFRYYFDSWGQGTLVTVS SASTKG 291 3A966HC QTLSLTCSVSGGSISSAGYYWGWIRQHPGKGLEWIGHIYYSGNTNYNPS LKSRLSMSVETSKNQFSLNLASVTAADTAVYFCARDYSAAGRHLFDSWG QGILVTVSSASTKG 292 3A978HC KPSQTLSLTCTVSGGSISSAGYYWTWIRHHPGKGLEFIGYIYHIGTPYYN PSLKSRLTISIDTSKNQFSLKLSSVTAADTAIYYCARDYTARGRHFFDYW GQGALVTVSSASTKG 293 3ANC3HC QVQLVQSGADVKKPGASVTVSCKTDEDEDDFRAHLVQWMRQAPGQRL EWVGWIKPQTGQPSYAQKFQGRVTLTREVSTSTVFLQLRNLRSDDTAV YYCARPRGGRDNWSFHVWGRGTLVTVSSASTKG 294 3ANC42HC QVQLVQSGAAVKKPGASVKVSCETYGYTFTDHFMHWWRQAPGQGLE WMGWINPYSSAVSYSPRYQGRVTMTRDTFLETVYMELRGLKFDDTAIYY CATPKSGRDYWSFDLWGQGTLVTVSSASTKG 295 3ANC66HC QVQLVQSGAAVKKPGASVKVSCETYGYKFTDHFMHWWRQAPGQGLE WMGWINPYSSAVSYSPRYQGRVTMTRDTFLETVYMELRGLRFDDTAIY YCATPKSGRDYWSFDLWGQGTLVTVSSASTKG 296 3ANC79HC QVQLVQSGAAVKKPGASVKVSCEAYGYKFTDHFMHWWRQAPGQGLE WMGWINPYTSAVNYSPKYQGRVTMTRDTFLETVYMELRGLRVDDTAIY YCATPKSGRDYWSFDLWGQGTLVTVSSASTKG 297 3B10HC QVQLQESGPGLVKPSETLSLTCSVSNGSISSGGYYWSWLRQFPGKGLE WIGSIHYTGRTMYNPSLMGRPALSMDTSNNQFSLKLRSVTAADTALYFC ARDLQWIFVVDPWGQGTLVTVSSASTKG 298 3B120HC LQQLQVPRLSMWRVFKVAAATGAQTLTVEEPGSSVKVSCKASGGSSTA YGYSWVRQAPGQGFEWMGRIIPFYGIITYAPKFQGRVTITADRSTSTVYM ELTSLTFADTALFFCARDFGDPRNGYYFDSWDQGLWLTVSSASTKG 299 3B126HC QVHLVQSGAEVKKPGSSVRVSCKASGWTFGDSVNSAITWVRQAPGQG LEWMGRFIPILGLSNYAQKFQDRVTINVDRSTNTAYMELSGLRSEDTAVY YCARLITGMNAPWFYYMDVWGKGTTITVSSASTKG 300 3B129HC FICFSVWVRLLEFGGRLVQPGGSLRLSCSASGFTFSNSAMSWVRQAPGK GLEWVSSILSSGVGTFYADSVKGRFTVSRDNSRNTLYLQMKSLRAEDTA LYYCAKVQIQQLNFGVITDAGLDVWGKGTTLIVSSASTKG 301 3B142HC QVQLGQSGTEVKKPGFSVKVSCKASGGSSTAYGYSWVRQAPGQGFEW MGRIIPFYGIITYAPKFQGRVTITADRSTSTVYMELTSLTFADTALFFCARD FGDPRNGYYFDSWDQGLWLTVSSASTKG 302 3B154HC QVQLVQSGGEVRKPGSSVKVPCKISGNAFSNYGVNWVRQAPGQGLEW VGRIIPVIGVAQHAPKFQGRVTITADKSTTTAYLELSSLRSDDTAVYFCAK DHGDPRTGYYFDYWGQGALVTVSSASTKG 303 3B165HC QVQLLQSGTEVKKPGSSVKVSCRASGWTLGNSPNSAIGWVRQAPGQG LEWIGRIIPILDVTNYAQKFQGRVTISADKSTNIAYMEISSLGSEDTAFYYC ARVITGMTSPWYFYMDVWGEGTTVIVSSASTKG 304 3B171HC VQSQVYLVQSGGEVKKPGSSVKVSCKASGDSFSSSVITWVRQAPGQGP EWMGRIIPVLGVAAYAQNFYGRVTISADTSSNTAYMELSSLRFEDTAVFY CARETGRGGNLALRQYFFDSWGQGTLVTVSSPSTKG 305 3B17HC EVQLVESGGGLVQPGGSLRISCSATGFTFSTHAMHWVRQAPGKGLEYV SAINSNGRSAFYADSVKGRVTISRDNSKNTLFLQMTSLRAEDTAVYYCVK GPLLRYLDSWGQGTLVTVSSASTKG 306 3B186HC QVQLVESGGGLVKPGGSLRLSCAASGFSFNEYYMSWIRQAPGQGLEW VANIGSSDAYTIYADSVKGRFTISRDNAENTVYLQMNSLRGEDTAVYYCA RIEGYCSNSRCSNYFDPWGQGALVTVSSASTKG 307 3B193HC MFLFLVAGATGVQSQVYLVPFGPEVKKPGSSVKVSCKASGDSFTSSVIT WVRQAPGQGPEWMGRVIPVLGVAAYAQKFYGRVTITADTSSNTAYMEV NSLRFEDTAVYYCARETGRGGNLALRQYFFDSWGQGTLVTVSSPSTKG 308 3B22HC CQVQLVESGGGWQPGRSLRLSCVGSGFTFSSSGMHWVRQAPGKGLE WVAVISSDGSDEYYGDSVEGRFTISRDNSKNTLFLQLDSLEAEDSAVYY CAKTPPHYDALTGYPSSVLEFWGLGTLVTVSSASTKG 309 3B27HC EVQLVESGGGLVQPGGSLRISCSATGFTFSTHAMHWVRQAPGKGLEYV SAINSNGRSAFYADSVKGRVTISRDNSKNTLFLQMTSLRAEDTAVYYCVK GPLLRYLDSWGQGTLVTVSSASTKG 310 3B29HC QVHLVQSGAEVKKPGSSVRVSCKASGWTFGDSVNSAITWVRQAPGQG LEWMGRFIPILGLSNYAQKFQDRVTINVDRSTNTAYMELSGLRSEDTAVY YCARLITGMNAPWFYYMDVWGKGTTITVSSASTKG 311 3B2HC SGGRLVQPGGSLRLSCSASGFTLSNSAMSWVRQAPGKGLEWVSSILSS GVGTFYADSVKGRFTVSRDNSRNTLYLQMKSLRAEDTALYYCAKVQIQQ LNFGVITDAGLDVWGKGTTLIVSSASTKG 312 3B31HC EVQLVQSGAEVKKPGSSVKVSCKASGGTFTTYDISWRQAPGQGLEWI GGILPDFGAPSYAQKFQDRVTITTDESSRTAYMELNSLRSEDTAIYYCAR GRGDDFWSGESPSWYFDYWGQGTQVTVSSASTKG 313 3B33HC PLVQLEPSGVEVKKRGASVKVSCKVSGYSLTELSMHWRQAPGKGLE WMGSFDPLDGDTIYAQKFQGRVTMTVDTSTDTAYMDLSSLRFEDTAVY YCATPSKAYYYDSPNYEGDFYMDVWGKGTTVIVSSASTKG 314 3B40HC QVQLVESGGGVVQPGRSLRLSCVGSGFTFSSSGMHWRQAPGKGLE WVAVISSDGSDEYYGDSVEGRFTISRDNSKNTLFLQLDSLEAEDSAVYY CAKTPPHYDALTGYPSSVLEFWGLGTLVTVSSASTKG 315 3B41HC EVQLVQSGAEVKKPGASVKVSCKVSGYTLTELSMHWRQAPGKGLEW MGVFDPLEGDGVYAEKFRGRVIMTEDTSTDTGYMELTSLRSEDTAIYYC ATKAKDYYYESSDYSPYYYYYMDVWGKGTTVTVSSASTKG 316 3B44HC EVRLLESGGGLVQPGGSLRLSCSASGFTFSNSALSWRQAPGKGLEW SSVSSGGDTFYADSVKGRFTISRDNSRNTLYLQMKSLRAEDTALYYCA KVQIQQLNFGVITDAGMDWWGKGTTVIVSSASTKG 317 3B45HC VEEPGSSVKVSCKASGGSSTAYGYSWRQAPGQGFEWMGRIIPFYGIIT YAPKFQGRVTITADRSTSTVYMELTRLTFADTALFFCARDYGDPRNGYY FDSWDQGLWLTVSSASTKG 318 3B48HC QVQLVESGGGLVQPGGSLRISCSATGFTFSTHAMHWVRQAPGKGLEYV SAINSNGRSAFYADSVKGRVTISRDNSKNTLFLQMTSLRAEDTAVYYCVK GPLLRYLDSWGQGTLVTVSSASTKG 319 3B50HC QVQLVQSGPGLVKPSETLSLTCSVSNGSISSGGYYWSWLRQFPGKGLE WIGSIHYTGRTFYNPSLMGRTALSMDTSNNQFSLKVSSVTAADTALYYC ARELQWMFWDPWGQGTLVTVSSASTKG 320 3B51HC QVQLLQSGTEVKKPGSSVKVSCRASGWTLGNSPNSAIGWVRQAPGQG LEWIGRIIPILDVTNYAQKFQGRVTISADKSTNIAYMEISSLGSEDTAFYYC ARVITGMTSPWYFYMDVWGEGTTVIVSSASTKG 321 3B56HC QVQLVQSGGEVKKPGASVKVSCKVSGYSLTELSMHWVRQAPGKGLEW MGVFDPLEGDGVYVQKFRGRVIMTEDTSTDTAYMELTSLRSEDTAIYYC ATKAKDYYYESSDYSPYYYYYMDVWGKGTTVTVSSASTKG 322 3B57HC GSEVQLVESGAEVKKRGASVKVSCKVSGYSLTELSMHWVRQAPGKGLE WMGSFDPLDGDTIYAQKFQGRVTMTVDTSTDTAYMDLSSLRFEDTAVY YCATPSKAYYYDSPNYEGDFYMDVWGKGTTVIVSSASTKG 323 3B5HC SVVQLVESGPGLVKPSETLSLTCSVSNGSISSGGYYWSWLRQFPGKGL EWIGSIHYTGRTMYNPSLMGRPALSMDTSNNQFSLKLRSVTAADTALYF CARDLQWIFVVDPWGQGTLVTVSSASTKG 324 3B61HC SVDERLLEFGGRLVQPGGSLRLSCSASGFTFSNSAMSWRQAPGKGLE WVSSILSSGVGTFYADSVKGRFTVSRDNSRNTLYLQMKSLRAEDTALYY CAKVQIQQLNFGVITDAGLDVWGKGTTLIVSSASTKG 325 3B6HC QLQLKESGPGMVKPSETLSLTCSVSGASVVSANDYWGWIRQAPGKGLE CIGIILYTGSTFYNPSLQSRVTISRDPSKNHVSLTLTSVTAADSAVYYCARI PYHSESYYNVVIGGFDVWGQGTRVTVSSASTKG 326 3B77HC QVHLVQSGAEVKKPGSSVRVSCKASGWTFGDSVNSAITWVRQAPGQG LEWMGRFIPILGLSNYAQKFQDRVTINVDRSTNTAYMELSGLRSEDTAVY YCARLITGMNAPWFYYMDVWGKGTTITVSSASTKG 327 3B79HC QVQLGQSGTEVKKPGFSVKVSCKASGGSSTAYGYSWVRQAPGQGFEW MGRIIPFYGIITYAPKFQGRVTITADRSTSTVYMELTSLTFADTALFFCARD FGDPRNGYYFDSWDQGLWLTVSSASTKG 328 3B84HC SQVQLVESGPGLVKPSETLSLTCSVSNGSISSGGYYWSWLRQFPGKGL EWIGSIHYTGRTMYNPSLMGRPALSMDTSNNQFSLKLSSVTAADTALYF CARDLQWIFVVDPWGQGTLVTVSSASTKG 329 3B86HC RVHSQVQLVESGPGLVKPSQTLSLTCTVSGGSISNGGHYWNWIRQHPG KGLEWIGHIYNIATTYYNPSLKSRVSISVDTSKNQFSLKLSSVTAADTAVY YCARGSGRWTIGARIYFDNWGQGALVAVSSASTKG 330 3B8HC QVQLVQSGGEVRKPGSSVKVPCKISGNAFSNYGVNWVRQAPGQGLEW VGRIIPVIGVAQHAPKFQGRVTITADKSTTTAYLELSSLRSDDTAVYFCAK DHGDPRTGYYFDYWGQGALVTVSSASTKG 331 3B93HC QVHLVQSGAEVKKPGSSVRVSCEASGWTFGSVNSAITWVRQAPGQGL EWMGRTIPFLGISNYAQKFQGRVTITADKSTNIAYVDVTSLTSQDTAVYY CARLITGMTAPWFYYMDVWGKGTTVTVSSASTKG 332 3BNC101HC EVQLVQSGSDVKKPGTTVTISCKADEDEDDFTAYNYFMHWVRQAPGQG LEWIGWINPRTGQPNHAKQLQGRVTLTRERSTSTVFMKLTNLRLDDTAV YFCARPLRGGDTWHYHSWGRGTSLIVSSASTKG 333 3BNC124HC QSQVHLVQSGAEVKKPGSSVKVSCQASGGTFNTFAINWVRQAPGQGLE WVGGIIPVFGTASYAQKFQGRVTVTTDESRGTAYMELNSLRSEDTAVYY CARGQTDLNDDLWSDYSTPGFDYWGQGTLVTVSSASTKG 334 3BNC130HC RVQLGQSGAEVKKPGASVKVSCKVSGNSLTEFSIHWVRQAPGKGLEW MGGFDPEEGETVPAQKFKGRVTMTEDTSTNTAYMELSSLRSEDTAVYY CSTEPREMGTLTAGFEYWGQGTLVIVSSASTKG 335 3BNC149HC QPQLVQSGSGAEVKKPGASVRISCEASEYNVFDHFMQWVRQAPMEGL EWMGWINPRGGYPSYSPTFQGRLTFTRQPSWDDSTITFHMELRGLRHD DTAVYYCARPHSPDDAWSLDVWGRGTLVTVSSASTKG 336 3BNC177HC LQPRVHSEVQLVESGAEVKKPGASVKVSCKVSGYTLSDLSMHWVRQAP GKGLEWMGGFDEEDGEITYAQKFQGRVSMTEDTSRDTAYMELSSLRSE DTAVYYCATAPRLELGELSSGFHYWGLGTLVTVSSASTKG 337 3BNC17HC RVQLGQSGAEVKKPGASVKVSCKVSGNSLTEFSIHWVRQAPGKGLEW MGGFDPEEGETVPAQKFKGRVTMTEDTSTNTAYMELSSLRSEDTAVYY CSTEPREMGTLTAGFEYWGQGTLVIVSSASTKG 338 3BNC48HC IWAPLIAVTFLVLHCESLGTCCCCQASGGTFNTFAINWVRQAPGQGLEW VGGIIPVFGTASYAQKFQGRVTVTTDESRGTAYMELNSLRSEDTAVYYC ARGQTDLNDDLWSDYSTPGFDYWGQGTLVTVSSASTKG 339 3BNC58HC EVQLVESGAEVKKPGASVKVSCKVSGYTLSDLSMHWVRQAPGKGLEW MGGFDEEDGEITYAQKFQGRVSMTEDTSRDTAYMELSSLRSEDTAVYY CATAPRLELGELSSGFHYWGLGTLVTVSSASTKG 340 3BNC78HC EVQLVESGAEVKKPGASVKVACKVSGKKLSDLSIHWVRQAPGKGLEWM GGFDEEDGKISYERKFQGRVTMTEDTARDTAFMEMSSLRSDDTAVYFC AAAPRLDLGELSSGFHFWGLGTLVSVSSASTKG 341 3BNC82HC CNPRVHSEVQLVESGAEVKKPGASVKVACKVSGKKLSDLSIHWVRQAP GKGLEWMGGFDEEDGKISYERKFQGRVSMTEDTARDTAFMEMSSLRS DDTAVYFCAAAPRLDLGELSSGFHFWGLGTLVTVSSASTKG 342 3BNC8HC EVQLVESGAEVKKPGASVKVSCKVSGNSLTEFSIHWVRQAPGKGLEWM GGFDPEEGETVPAQKFKGRLTMTEDTSTNTAYMELSSLRSEDTAVYYCS TEPREMGTLTAGFEYWGQGTLVTVSSASTKG 343 3a426hc QVQLQESGPGLVKPSETXSLTCSVSNGSISSGGYYWSWLRQFPGKGLE WIGSIHYTGRTMYNPSLMGRPALSMDTSNNQFSLKLSSVTAADTALYFC ARDLQWIFVVDPWGQGTLVTVSSASTKG 344 3a515hc QVQLVQSGAEVKKPGSSVKVSCKASGGTFTTYDISWRQAPGQGLEW MGGILPDFGAPSYAQKFQDRVTITTDESSSTAYMELNSLRSEDTAIYYCA RGRGDDFWSGESPSWYFDYWGQGTLVTVSSASTKG 345 3b46HC GYSEVQLVQSGPGLVKPSQTLSLTCTVSGGSISNGGHYWNWIRQHPGK GLEWIGHIYNIATTYYNPSLKSRVSISVDTSKNQFSLKLSSVTAADTAVYY CARGSGRWTIGARIYFDNWGQGALVAVSSASTKG 346 3ANC32HC QVQLVQSGADVKKPGATVTVSCKTDEDEDDFRAHLMQWMRQAPGQRL EWVGWIKPQTGQPSYGQKFQGRVTLTREVSTSTVFLQLRNLRSDDTAV YYCARPRGGRDNWSFHVWGRGTLVTVSSASTKG 347 3ANC3HC QVQLVQSGADVKKPGASVTVSCKTDEDEDDFRAHLVQWMRQAPGQRL EWVGWIKPQTGQPSYAQKFQGRVTLTREVSTSTVFLQLRNLRSDDTAV YYCARPRGGRDNWSFHVWGRGTLVTVSSASTKG 348 3ANC41HC QVQLVQSGAAVKKPGASVKVSCETYGYTFTDHFMHWWRQAPGQGLE WMGWINPYSSAVSYSPRYQGRVTMTRDTFLETVYMELRGLKFDDTAIYY CATPKSGRDYWSFDLWGQGTLVTVSSASTKG 349 3ANC42HC QVQLVQSGAAVKKPGASVKVSCETYGYTFTDHFMHWWRQAPGQGLE WMGWINPYSSAVSYSPRYQGRVTMTRDTFLETVYMELRGLKFDDTAIYY CATPKSGRDYWSFDLWGQGTLVTVSSASTKG 350 3ANC66HC QVQLVQSGAAVKKPGASVKVSCETYGYKFTDHFMHWWRQAPGQGLE WMGWINPYSSAVSYSPRYQGRVTMTRDTFLETVYMELRGLRFDDTAIY YCATPKSGRDYWSFDLWGQGTLVTVSSASTKG 351 3ANC70HC QVQLVQSGAAVKKPGASVKVSCETYGYKFTDHFMHWWRQAPGQGLE WMGWINPYSSAVSYSPRYQGRVTMTRDTFLETVYMELRGLRFDDTAIY YCATPKSGRDYWSFDLWGQGTLVTVSSASTKG 352 3ANC75HC QVQLVQSGAAVKKPGASVKVSCETYGYTFTDHFMHWWRQAPGQGLE WMGWINPYSSAVSYSPRYQGRVTMTRDTFLETVYMELRGLKFDDTAIYY CATPKSGRDYWSFDLWGQGTLVTVSSASTKG 353 3ANC79HC QVQLVQSGAAVKKPGASVKVSCEAYGYKFTDHFMHWWRQAPGQGLE WMGWINPYTSAVNYSPKYQGRVTMTRDTFLETVYMELRGLRVDDTAIY YCATPKSGRDYWSFDLWGQGTLVTVSSASTKG 354 3ANC87HC QVQLVQSGGAVKKPGASVKVSCETYGYTFTDHFMHWWRQAPGQGLE WMGWINPYSSAVSYSPRYQGRVTMTRDTFLETVYMELRGLKFDDTAIYY CATPKSGRDYWSFDLWGQGTLVTVSSASTKG 355 3ANC8HC QVQLVQSGADVKKPGASVTVSCKTDEDEDDFRAHLVQWMRQAPGQRL EWVGWIKPQTGQPSYAQKFQGRVTLTREVSTSTVFLQLRNLRSDDTAV YYCARPRGGRDNWSFHVWGRGTLVTVSSASTKG 356 3ANC96HC QVQLVQSGADVKKPGASVTVSCKTDEDEDDFRAHLVQWMRQAPGQRL EWVGWIKPQTGQPSYAQKFQGRVTLTREVSTSTVFLQLRNLRSDDTAV YYCARPRGGRDNWSFHVWGRGTLVTVSSASTKG 357 3B106HC QVQLLQSGAAVTKPGASVRVSCEASGYNIRDYFIHWWRQAPGQGLQW VGWINPKTGQPNNPRQFQGRVSLTRHASWDFDTFSFYMDLKALRSDDT AVYFCARQRSDYWDFDVWGSGTQVIVSSASTKG 358 3B16HC QVQLLQSGAAVTKPGASVRVSCEASGYNIRDYFIHWWRQAPGQGLQW VGWINPKTGQPNNPCQFQGRVSLTRHASWDFDTFSFYMDLKALRSDDT AVYFCARQRSDYWDFDVWGSGTQVTVSSASTK 359 3B180HC QVQLLQSGAAVTKPGASVRVSCEASGYNIRDYFIHWWRQAPGQGLQW VGWINPKTGQPNNPCQFQGRVSLTRQASWDFDTISFYMDLKALRLDDT AVYFCARQRSDYWDFDVWGSGTQVTVSSASTKG 360 3B183HC QVRLLQSGAAVTKPGASVRVSCEASGYEIRDYFIHWWRQAPGQGLQWV GWINPKTGQPNNPRQFQGRVSLTRQASWDFDSYSFYMDLKALRSDDTA VYFCARQRSDYWDFDVWGSGSQVTVSSASTKG 361 3B191HC QVRLLQSGAAVTKPGASVRVSCEASGYEIRDYFIHWWRQAPGQGLQWV GWINPKTGQPNNPRQFQGRVSLTRQASWDFDSYSFYMDLKALRSDDT GVYFCARQRSDYWDFDVWGSGTQVTVSSASTKG 362 3B21HC QVRLLQSGAAVTKPGASVRVSCEASGYEIRDYFIHWWRQAPGQGLQWV GWINPKTGQPNNPRQFQGRVSLTRQASWDFDSYSFYMDLKALRSDDTA VYFCARQRSDYWDFDVWGSGTQVTVSSASTKG 363 3BBM60 QVHLSQSGAVVTKPGASVRVSCEASGYKISDHFIHWWRQAPGQGPQW VGWINPKTGQPNNPRQFQGRISLTRQASWDFDTFSFYMDLKALRSDDT AVYFCARHRSDYWDFDVWGSGTQVTVSSASTKG 364 3BBM60 QVHLSQSGAAVTKPGASVRVSCEASGYKISDHFIHWWRQAPGQGLQW VGWINPKTGQPNNPRQFQGRISLTRQASWDFDTFSFYMDLKALRSDDT AVYFCARQRSDYRDFDVWGSGTQVTVSSASTKG 365 3BBM60 QVHLSQSGAAVTKPGASVRVSCEASGYKIRDYSIHWWRQAPGQGLQW VGWINPQTGQPNIPRPFQGRISLTRQASWDFDTFSFYMDLEALRSDDTA VYFCARQRSDYWDFDVWGSGTQVTVSSASTKG 366 3BBM60 QVHLSQSGAVVTKPGASVRVSCEASGYKISDHFIHWWRQAPGQGLQW VGWINPKTGQPNNPRQFQGRISLTRQASWDFDTFSFYMDLEALRSDDT AVYFCARQRSDYWDFDVWGSGTQVTVSSASTKG 367 3BBM60 QVHLSQSGAVVTKPGASVRVSCEASGYKISDHFIHWWRQAPGQGLQW VGWINPKTGQPNNPRQFQGRISLTRQASWDFDTFSFYMDLKALRSDDT AVYFCARHRSDYWDFDVWGSGTQVTVSSASTKG 368 3BBM60 QVHLSQSGAAVTKPGASVRVSCEASGYKISDHFIHWWRQAPGQGLQW VGWINPKTGQPNNPRQFQGRVSLTRQASWDFDTYSFYMGLKAVRSDD TAIYFCARQRSDFWDFDVWGSGTQVTVSSASTKG 369 3BBM60 QVHLSQSGAAVTKPGASVRVSCEASGYKISDHFIHWWRQAPGQGLQW VGWINPKTGQPNNPRQFQGRISLTRQASWDFDTFSFYMDLKALRSDDT AVYFCARHRSDYWDFDVWGSGTQVTVSSASTKG 370 3BBM60 QVHLSQSGAVVTKPGASVRVSCEASGYKISGHFIHWWRQAPGQGLQW VGWINPKTGQPNNPRQFQGRISLTRQASWDFDTFSFYMDLKALRSDDT AVYFCARHRSDYWDFDVWGSGTQVTVSSASTKG 371 3BBM60 QVHLSQSGAVVTKPGASVRVSCEASGYKISDHFIHWWRQAPGQGLQW VGWINPKTGQPNIPRQFQGRISLTRQASGDFDTFSFYMDLKALRSDDTA VYFCARQRSDYWDFGVWGSGTQVTVSSASTKG 372 3BBM60 QVHLSQSGAVVTKPGASVRVSCEASGYKISDHFIHWWRQAPGQGLQW VGWINPKTGQPNNPRQFQGRISLTRQASWDIDTFSFYMDLKALRSDDTA VYFCARHRSDYWDFDVWGSGTQVTVSSASTKG 373 3BBM60 QVHLSQSGAVVTKPGASVRVSCEASGYKISDHFIHWWRQAPGQGLQW VGWINPKTGQPNNPRQFQGRISLTRQASWDFDTFSFYMDLKALRSDDT AVYFCARQRSDYWDFDVWGSGTQVTVSSASTKG 374 3BBM60 QVHLSHSGAAVTKPGASVRVSCEASGYKISDHFIHWWRQAPGQGLQW VGWINPKTGQPNNPRQFQGRISLTRQASWDFDTFSFYMDLKALRSDDT AVYFCARQRSDYWDFDVWGSGTQVTVSSASTKG 375 3BBM60 QVHLSQSGAVVTKPGASVRVSCEASGYKISDHFIHWWRQAPGQGLQW VGWINPKTGQPNNPRQFQGRISLTRQASWDFDTFSFYMDLKALRSDDT AVYFCARHRSDYWDFDVWGSGTQVTVSSASTKG 376 3BBM60 QVHLSQSGAVVTKPGASVRVSCEASGYKISDHFIHWWRQAPGQGLQW VGWINPKTGQPNNPRQFQGRISLTRQASWDFDTFSFYMDLKALRSDDT AVYFCARHRSDYWDFDVWGSGTQVTVSSASTKG 377 3BBM60 QVHLSQSGAAVTKPGASVRVSCEASGYKISDHFIHWWRQAPGQGLQW VGWINPKTGQPNNPRQFQGRISLTRQASWDFDTFSFYMDLKALRSDDT AVYFCARHRSDYWDFDVWGSGTQVTVSSASTKG 378 3BNC101HC EVQLVQSGSDVKKPGTTVTISCKADEDEDDFTAYNYFMHWRQAPGQG LEWIGWINPRTGQPNHAKQLQGRVTLTRERSTSTVFMKLTNLRLDDTAV YFCARPLRGGDTWHYHSWGRGTSLIVSSASTKG 379 3BNC102HC QPQLVQSGSGAEVKKPGASVRISCEASEYNVFDHFMQWRQAPGQGL EWMGWINPRGGYPSYSPRFQGRLTFTRQPSWDDSSVTFHMELRGLRH DDTAVYYCARPHSPDDAWSLDVWGRGTLVTVSSASTKG 380 3BNC104HC EVQLVQSGSDVRKPGATVTVSCKADEDEDDFTAYNYFMHWRQAPGH GLEWIGWINPRTGQPNHAKQFQGRVTLTRERSTSTVFMKLTNLRLDDTA VYFCARPLRGGDTWHYHSWGRGTSLTVSSASTKG 381 3BNC105HC HVQLLQSGAAVTKPGASVRVSCEASGYNIRDYFIHWWRQAPGQGLQW VGWINPKTGQPNNPRQFQGRVSLTRQASWDFDTFSFYMDLKALRLDDT AIYFCARQRSDYWDFDVWGSGTQVTVSSASTKG 382 3BNC106HC VVQLVQSGSDVRKPGATVTVSCKADEDEDDFTAYNYFMHWVRQAPGH GLEWIGWINPRTGQPNHAKQFQGRVTLTRERSTSTVFMKLTNLRLDDTA VYFCARPLRGGDTWHYHSWGRGTSLTVSSASTKG 383 3BNC107HC QVQLVQSGAALKKPGASLRISCQAYGYKFTDYLIHWWRQAPGQGLEWI GWIKPETGQPSYSYKFQGRVSLTRDTFEEILFMDLRGLRSDDTAIYFCAR RHSDYCDFDVWGGGSQVLVSSASTKG 384 3BNC108HC QVQLVQSGTAVKKPGASVRVSCQASGYTFTDYFIYWWRQAPGQGLEW LGWINPRTSQPSYPYRFQGRVTLTRDIFEEMLYMDLRGLRSDDTGIYFC ARRHSDYCDFDIWGSGTQIIVSSASTKG 385 3BNC10HC EVQLVQSGSDVRKPGATVTVSCKADEDEDDFTAYNYFMHWVRQAPGH GLEWIGWINPRTGQPNHAKQFQGRVTLTRERSTSTVFMKLTNLRLDDTA VYFCARPLRGGDTWHYHSWGRGTSLTVSSASTKG 386 3BNC114HC EVQLVQSGSDVRKPGATVTVSCKADEDEDDFTAYNYFMHWVRQAPGH GLEWIGWINPRTGQPNHAKQFQGRVTLTRERSTSTVFMKLTNLRLDDTA VYFCARPLRGGDTWHYHSWGRGTSLTVSSASTKG 387 3BNC117HC QVQLLQSGAAVTKPGASVRVSCEASGYNIRDYFIHWWRQAPGQGLQW VGWINPKTGQPNNPRQFQGRVSLTRHASWDFDTFSFYMDLKALRSDDT AVYFCARQRSDYWDFDVWGSGTQVTVSSASTKG 388 3BNC126HC QPQLVQSGSGAEVKKPGASVRISCEASEYNVFDHFMQWVRQAPGQGL EWMGWINPRGGYPSYSPTFQGRLTFTRQPSWDDSTITFHMELRGLGHD DTAVYYCARPHSPDDAWSLDVWGRGTLVTVSSASTKG 389 3BNC127HC EVQLVESGSDVRKPGATVTVSCKADEDEDDFTAYNYFMHWRQAPGQ GLEWIGWINPRTGQPNHAKQFQGRVTLTRERSTSTVFMKLTNLRLDDTA VYFCARPLRGGDTWHYHSWGRGTSLTVSSASTKG 390 3BNC134HC QVQLVQSGAALKKPGASLRISCQAYGYKFTDHLIYWWRQAPGQGLEWI GWIKPETGQPSYSYKFQGRVSLTRDTFQEILFMNLRGLRSDDTAIYFCAR RHSDYCDFDVWGSGSQILVSSASTKG 391 3BNC140HC EVQLVQSGSDVRKPGATVTVSCKADEDEDDFTAYNYFMHWVRQAPGH GLEWIGWINPRTGQPNHAKQFQGRVTLTRERSTSTVFMKLTNLRLDDTA VYFCARPLRGGDTWHYHSWGRGTSLTVSSASTKG 392 3BNC141HC VVQLVQSGSDVRKPGATVTVSCKADEDEDDFTAYNYFMHWVRQAPGH GLEWIGWINPRTGQPNHAKQFQGRVTLTRERSTSTVFMKLTNLRLDDTA VYFCARPLRGGDTWHYHSWGRGTSLTVSSASTKG 393 3BNC142HC QVQLVQSGAALKKPGASVRISCQAYGYKFTDHLIYWWRQAPGQGLEWI GWIKPETGQPSYSYKFQGRVTLTRDTFEEIHFMDLRGLRYDDTATYFCA RRHSDYCDFDVWGSGSQVSVSSASTKG 394 3BNC148HC QVQLVQSGSDVRKPGATVTVSCKADEDEDDFTAYNYFMHWVRQAPGH GLEWIGWINPRTGQPNHAKQFQGRVTLTRERSTSTVFMKLTNLRLDDTA VYFCARPLRGGDTWHYHSRGRGTSLTVSSASTKG 395 3BNC149HC QPQLVQSGSGAEVKKPGASVRISCEASEYNVFDHFMQWVRQAPMEGL EWMGWINPRGGYPSYSPTFQGRLTFTRQPSWDDSTITFHMELRGLRHD DTAVYYCARPHSPDDAWSLDVWGRGTLVTVSSASTKG 396 3BNC151HC QVQLVQSGATLKKPGASVRISCQAYGYKFTDHLIHWWRQAPGQGLEWI GWIKPETGQPSYAYKFQGRVSLTRDTFEEILFMDLRGLRSDDTAIYFCAR RHSDYCDLDVWGGGTQLLVSSASTKG 397 3BNC153HC QVQLVQSGAALKKPGASLRISCLTYGYKFTDHLIYWWRQAPGQGLEWIG WIKPETGQPSYSYRFQGRVSLTRDTFEEIVFMDLRGLRSDDTAIYFCARR HSDYCDFDVWGSGSQVIVSSASTKG 398 3BNC156HC QVQLVQSGAALKKPGASLRISCQTYGYKFTDHLIYWWRQAPGQGLEWI GWIKPETGQPSYSYRFQGRVSLTRDTFEEIVFMDLRGLRSDDTAIYFCAR RHSDYCDFDVWGGGSQVIVSSASTKG 399 3BNC158HC QVQLVQSGAALKKPGASLRISCQTYGYKFTDHLIYWWRQAPGQGLEW GWIKPETGQPSYSYRFQGRVSLTRDTFEEIVFMDLRGLRSDDTAIYFCAR RHSDYCDFDVWGSGSQVIVSSASTKG 400 3BNC159HC QVQLVQSGAALKKPGASVRISCQTYGYKFTDHLIHWWRQAPGQGLEWI GWIKPDTGQPSYSSRFQGRVSLTRDTFEEIVFMDLRGLRSDDTAIYFCA RRHSDYCDFDVWGSGSQVLVSSASTKG 401 3BNC15HC QVQLVQSGAALKKPGASLRISCQTYGYKFTDHLIYWWRQAPGQGLEWI GWIKPETGQPSYSYRFQGRVSLTRDTFEEIVFMDLRGLRSDDTAIYFCAR RHSDYCDFDVWGSGSQVLVSSASTKG 402 3BNC173HC QVQLVQSGSDVRKPGATVTVSCKADEDEDDFTAYNYFMHWRQAPGH GLEWIGWINPRTGQPNHAKQFQGRVTLTRERSTSTVFMKLTNLRLDDTA VYFCARPLRGGDTWHYHSWGRGTSLTVSSASTKG 403 3BNC175HC EVQLVQSGSDVRKPGATVTVSCKADEDEDDFTAYNYFMHWVRQAPGH GLEWIGWINPRTGQPNHAKQFQGRVTLTRERSTSTVFMKLTNLRLDDTA VYFCARPLRGGDTWHYHSWGRGTSLTVSSASTKG 404 3BNC176HC QVQLLQSGAAVTKPGASVRVSCEASGYNIRDYFIHWWRQAPGQGLQW VGWINPKTGQPNNPRQFQGRVSLTRHASWDFDTFSFYMDLKGLRSDDT AIYFCARQRSDYWDFDVWGSGTQVTVSSASTKG 405 3BNC181HC EVQLVQSGSDVRKPGATVTVSCKADEDEDDFTAYDYFMHWVRQAPGH GLEWIGWINPRTGQPNHAKQFQGRVTLTRERSTSTVFMKLTNLRLDDTA VYFCARPLRGGDTWHYHSWGRGTSLTVSSASTKG 406 3BNC186HC EVQLVQSGSDVRKPGATVTVSCKADEDEDDFTAYNYFMHWVRQAPGH GLEWIGWINPRTGQPNHAKQFQGRVTLTRERSTSTVFMKLTNLRLDDTA VYFCARPLRGGDTWHYHSWGRGTSLTVSSASTKG 407 3BNC18HC EVQLVQSGSDVRKPGATVTVSCKADEDEDDFTAYNYFMHWVRQAPGH GLEWIGWINPRTGQPNHAKQFQGRVTLTRERSTSTVFMKLTNLRLDDTA VYFCARPLRGGDTWHYHSWGRGTSLTVSSASTKG 408 3BNC193HC QVQLVQSGTAVKKPGASVRVSCQASGYTFTDYFIYWWRQAPGQGLEW LGWINPRTSQPSYPYRFQGRVTLTRDIFEEMLYMDLRGLRSDDTGIYFC ARRHSDYCDFDIWGSGTQIIVSSASTKG 409 3BNC196HC QVQLLQSGAAVTKPGASVRVSCEASGYKISDHFIHWWRQAPGQGLQW VGWINPKTGQPNNPRQFQGRISLTRQASWDFDTFSFYMDLKALRSDDT AVYFCARQRSDYWDFDVWGSGTQVTVSSASTKG 410 3BNC20HC QVQLVQSGSDVRKPGATVTVSCKADEDEDDFTAYNYFMHWVRQAPGH GLEWIGWINPRTGQPNHAKQFQGRVTLTRERSTSTVFMKLTNLRLDDTA VYFCARPLRGGDTWHYHSWGRGTSLTVSSASTKG 411 3BNC29HC VVQLVQSGSDVRKPGATVTVSCKADEDEDDFTAYNYFMHWVRQAPGH GLEWIGWINPRTGQPNHAKQFQGRVTLTRERSTSTVFMKLTNLRLDDTA VYFCARPLRGGDTWHYHSWGRGTSLTVSSASTKG 412 3BNC31HC QVQLVQSGAALKKPGASVRISCQTYGYKFTDHLIYWWRQAPGQGLEWI GWIKPETGQPSYSYRFQGRVSLTRDTFEEIVFMDLRGLRSDDTAIYFCAR RHSDYCDFDVWGSGSQVLVSSASTKG 413 3BNC33HC VVQLVQSGSDVRKPGATVTVSCKADEDEDDFTAYNYFMHWVRQAPGH GLEWIGWINPRTGQPNHAKQFQGRVTLTRERSTSTVFMKLTNLRLDDTA VYFCARPLRGGDTWHYHSWGRGTSLTVSSASTKG 414 3BNC42HC QVQLVQSGAALKKPGASVRISCQAYGYKFTDYLIHWWRQAPGQGLEWI GWIKPETGQPSYSYKFQGRVTLTRDTFEEILFMDLRGLRSDDTAIYFCAR RHSDYCDFDVWGSGSQVIVSSASTKGA 415 3BNC44HC EVQLVESGSDVRKPGATVTVSCKADEDEDDFTAYNYFMHWVRQAPGH GLEWIGWINPRTGQPNHAKQFQGRVTLTRERSTSTVFMKLTNLRLDDTA VYFCARPLRGGDTWHYHSWGRGTSLTVSSASTKG 416 3BNC45HC VVQLVQSGSDVRKPGATVTVSCKADEDEDDFTAYNYFMHWVRQAPGH GLEWIGWINPRTGQPNHAKQFQGRVTLTRERSTSTVFMKLTNLRLDDTA VYFCARPLRGGDTWHYHSWGRGTSLTVSSASTKG 417 3BNC53HC QVQLVQSGAALKKPGASVRISCQAYGYKFTDHLIYWWRQAPGQGLEWI GWIKPETGQPSYAYKFQGRVTLTRDTFEEIHFMDLRGVRNDDTATYFCA RRHSDYCDFDVWGSGSQVIVSSASTKG 418 3BNC54HC EVQLVESGSDVRKPGATVTVSCKADEDEDDFTAYNYFMHWVRQAPGH GLEWIGWINPRTGQPNHAKQFQGRVTLTRERSTSTVFMKLTNLRLDDTA VYFCARPLRGGDTWHYHSWGRGTSLTVSSASTKG 419 3BNC55HC QVQLVQSGTAVKRPGASVRVSCQASGYTFTDYFIYWWRQAPGQGLEW LGWINPLTSQPSYPSRFQGRLTLTRDTFDEMLYMDLRGLRSDDTGIYFC ARRHSDYCDFDIWGSGTQIIVSSASTKG 420 3BNC59HC EVQLVQSGSDVRKPGATVTVSCKADEDEDDFTAYNYFMHWVRQAPGH GLEWIGWINPRTGQPNHAKQFQGRVTLTRERSTSTVFMKLTNLRLDDTA VYFCARPLRGGDTWHYHSWGRGTSLTVSSASTKG 421 3BNC60HC QVHLSQSGAAVTKPGASVRVSCEASGYKISDHFIHWWRQAPGQGLQW VGWINPKTGQPNNPRQFQGRVSLTRQASWDFDTYSFYMDLKAVRSDD TAIYFCARQRSDFWDFDVWGSGTQVTVSSASTKG 422 3BNC62HC QVRLLQSGAAVTKPGASVRVSCEASGYEIRDYFIHWWRQAPGQGLQW GWINPKTGQPNNPRQFQGRVSLTRQASWDFDSYSFYMDLKALRSDDT GVYFCARQRSDYWDFDVWGSGTQVTVSSASTKG 423 3BNC64HC QVHLSQSGAAVTKPGASVRVSCEASGYKISDHFIHWWRQAPGQGLQW VGWINPKTGQPNNPRQFQGRVSLTRQASWDFDTYSFYMDLKALRSDDT AIYFCARQRSDFWDFDVWGSGTQVTVSSASTKG 424 3BNC65HC QVQLLPFGGAVTKPGASVRVSCEASGYNIRDYFIHWWRQAPGQGLQW VGWINPKTGQPNNPCQFQGRVSLTRPASWDFDTISFYMDLKALRLDDTA VYFCARQRSDYWDFDVWGSGTQVTVSSASTKG 425 3BNC66HC QVQLVQSGAALKKPGASLRISCQTYGYKFTDHLIYWWRQAPGQGLEWI GWIKPETGQPSYSYRFQGRVSLTRDTFEEIAFMDLRGLRSDDTAIYFCAR RHTDYCVFDVWGSGSQIIVSSASTKG 426 3BNC6HC QVQLVESGSDVRKPGATVTVSCKADEDEDDFTAYNYFMHWRQAPGH GLEWIGWINPRTGQPNHAKQFQGRVTLTRERSTSTVFMKLTNLRLDDTA VYFCARPLRGGDTWHYHSWGRGTSLTVSSASTKG 427 3BNC72HC QVQLVQSGAALKKPGASLRISCQTYGYKFTDHLIYWWRQAPGQGLEWM GWIKPETGQPSYSYRFQGRVSLTRDTFEEIVFMDLRGLRSDDTAIYFCAR RHSDYCDFDVWGSGSQVIVSSASTKG 428 3BNC75HC QVQLLQSGAAVTKPGASVRVSCEASGYNIRDYFIHWWRQAPGQGLQW VGWINPKTGQPNNPRQFQGRVSLTRHASWDFDTFSFYMDLKALRSDDT AVYFCARQRSDYWDFDVWGSGTQVTVYSASTKG 429 3BNC79HC QVQLLQSGAAVTKPGASVRVSCEASGYNIRDYFIHWWRQAPGQGLQW VGWINPKTGQPNNPRQFQGRVSLTRQASWDFDTISFYMDLKALRLDDT AVYFCARQRSDYWDFDVWGSGTQVTVSSASTKG 430 3BNC81HC RQVQLVQSGAALKKPGASLRISCQAYGYKFTDHLIYWWRQAPGQGLEW IGWIKPETGQPSYSYKFQGRVSLTRDTFQEILFMDLRGLRSDDTAIYFCA RRHSDYCDFDVWGSGSQILVSSASTKG 431 3BNC84HC QVQLVQSGAALKKPGASLRISCQAYGYKFTDHLIYWWRQAPGQGLEWI GWIKPETGQPSYSYKFQGRVSLTRDTFQEILFMDLRGLRSDDTAIYFCAR RHSDYCDFDVWGSGSQVIVSSASTKG 432 3BNC86HC QVQLVQSGSDVRKPGATVTVSCKADEDEDDFTAYNYFMHWVRQAPGH GLEWIGWINPRTGQPNHAKQFQGRVTLTRERSTSTVFMKLTNLRLDDTA VYFCARPLRGGDTWHYHSWGRGTSLTVSSASTKG 433 3BNC87HC QVQLLQSGAAVTKPGASVRVSCEASGYNIRDYFIHWWRQAPGQGLQW VGWINPKTGQPNNPRQFQGRVSLTRHASWDFDTFSFYMDLKALRSDDT AVYFCARQRSDYWDFDVWGSGTQVTVSSASTKG 434 3BNC89HC QVQLVQSGTAVKRPGASVRVSCQASGYTFIDHFIYWWRQAPGQGLEWL GWINPLTSQPSYPSRFQGRLTLTRDTFDEMLYMDLRGLRSDDTGIYFCA RRHSDYCDFDIWGSGTQIIVSSASTKG 435 3BNC91HC QVQLLQSGAVVTKPGASVRVSCEASGYKIRDYFIHWWRQAPGQGLQW VGWINPQTGQPNIPRPFQGRVTLTRHASWDFDTFSFYMDLKALRSDDTA IYFCARRRSDYCDFDVWGSGTHVTVSSASTKG 436 3BNC92HC EVQLVQSGSDVRKPGATVTVSCKADEDEDDFTAYNYFMHWVRQAPGH GLEWIGWINPRTGQPNHAKQFQGRVTLTRERSTSTVFMKLTNLRLDDTA VYFCARPLRGGDTWHYHSWGRGTSLTVSSASTKG 437 3BNC94HC QVQLVQSGSDVRKPGATVTVSCKADEDEDDFTAYNYFMHWVRQAPGH GLEWIGWINPRTGQPNHAKQFQGRVTLTRERSTSTVFMKLTNLRLDDTA VYFCARPLRGGDTWHYHSWGRGTSLTVSSASTKG 438 3BNC95HC QVQLLQSGAAVTKPGASVRVSCEASGYNIRDYFIHWWRQAPGQGLQW VGWINPKTGQPNNPRLFQGRVSLTRHASWDFDTFSFYMDLKAVRSDDT AVYFCARQRSDYWDFDVWGSGTQVTVSSASTKG

TABLE B Seq ID No. Antibody Light Chain Amino Acid Sequence 439 8ANC131KC EIVLTQSPATLSLSPGERATLSCRASQGLNFVVWYQQKRGQAPRLLIH APSGRAPGVPDRFSARGSGTEFSLVISSVEPDDFAIYYCQEYSSTPYN FGPGTRVDRKRTVAAPSVFIFPPSDEQ 440 8ANC134KC EIVLTQSPATLSLSPGERATLSCRASQGLNFVVWYQQKGGQAPRLLIH GPTDRAPGVPDRFSARGSGTEFSLVISSVEPDDFALYYCQEYSSTPYN FGPGTRVDRKRTVAAPSVFIFPPSDEQ 441 8ANC13KC EIVLTQSPATLSLSPGERATLSCRASQGLNFVVWYQQKRGQAPRLLIH GPSHRAPGVPDRFSARGSGTEFSLVISSVEPDDFAIYYCQEYSSTPYN FGPGTRVDRKRTVAAPSVFIFPPSDEQ 442 8ANC45KC EIVLTQSPATLSLSPGERATLSCRASQGVNFVVWYQQKRGQAPRLLIY GPSNRAPGVPDRFSARGSGTEFSLVISSVEPDDFALYYCQEYSSTPYN FGPGTRVDRKRTVAAPSVFIFPPSDEQ 443 8ANC50KC EIVLTQSPTTLSLSPGERATLSCRASQGVNLVVWYQQKRGQAPRLLIY GPSDRAPGVPDRFSARGSGTEFSLVISSVEPDDFALYYCQEYSSTPYN FGTGTRVDRKRTVAAPSVFIFPPSDEQ 444 8ANC88KC EIVLTQSPATLSLSPGERATLSCRASQGLNFVVWYQQKRGQAPRLLIH APSDRAPGVPDRFSARGSGTDFSLVISSVEPDDFAIYYCQEYSSTPYN FGPGTRVDRKRTVAAPSVFIFPPSDEQ 445 8anc182kc EIVLTQSPATLSLSPGERATLSCRASQGVNFVVWYQQKRGQAPRLLIY GPSDRAPGVPDRFSARGSGTEFSLVISSVEPDDFALYYCQEYSSTPYN FGTGTRVDRKRTVAAP 446 8anc192kc EIVLTQSPATLSLSPGERATLSCRASQGVNFVVWYQQKRGQAPRLLIY GNSDRVPGVPDRFSARGSGTEFSLVISSVEPDDFALYYCQEYSSTPY NFGPGTRVDRKRTVAA 447 8ANC14KC SEIVLTQSPATLSLSPGERATLSCRASQSINNYLAWYQQKPGQAPRLLI YDASNRATGIPARFSGGGSGTDFTLTISSLEPEDFAVYYCQQRANWRL LTFGGGTKVEIKRTVAAPSVFIFPPSDEQ 448 8ANC16KC EIVMTQSPDTLSVSPGERATLSCRASQSVNSNLAWYQQKPGQAPRLLI YGASTRATAVPARFSGSGSGTEFTLTISSLQSEDSAVYYCQQYYQWL SYTFGQGTKLEIKRTVAAPSVFIFPPSDEQ 449 8ANC195KC DIQMTQSPSTLAASIGGTVRVSCRASQSITGNWVAWYQQRPGKAPRL LIYRGAALLGGVPSRFSGSAAGTDFTLTIGNLQAEDFGTFYCQQYDTY PGTFGQGTKVEVKRTVAAPSVFIFPPSDEQ 450 8ANC24KC SEIVMTQSPATLSMSPGERATLSCRASLSVNTNLAWYQQKPGQAPRL LIYGASTRATGIPARFSGSGSGTEFTLTISSLQSEDFALYYCQQYNHWP QTFGQGTKVEIKRTVAAPSVFIFPPSDEQK 451 8ANC5KC DIQMTQSPPSLSASVGDRVTITCQASQDINNFLNWYQQKPGKAPRLLI YDASNLESGVSSRFSGSRSGTDFTLTISSLLPEDIATYSCQQYSNLPYT FSQGTKLEIKRTVAAPSVFIFPPSDEQ 452 12a12kc DIQMTQSPSSLSASVGDRVTITCQAGQGIGSSLQWYQQKPGKAPKLL VHGASNLHRGVPSRFSGSGFHTTFSLTISGLQRDDFATYFCAVLEFFG PGTKVEIKRTVAAPSVFIFPPSDEQLKS 453 12a13kc DIQMTQSPSSLSASVGDRVTITCQAGQGIGSSLQWYQQKPGKAPKLL VHGASNLHRGVPSRFSGSGFHTTFSLTISGLQRDDFATYFCAVVEFFG PGTKVDIKRTVAAPSVFIFPPSDEQL 454 12a16kc DIQMTQSPSSLSASVGDRVTITCQASQGIGSSLQWYQQKPGRAPNLL VHGASKLHRGVPSRFSGSGFHTTFSLTISGLQRDDFATYFCAVLEFFG PGTKVEIKRTVAAPSVFIFPPSDEQLK 455 12a1kc DIQMTQSPSSLSASVGDRVSINCQAGQGLGSSLNWYQQKPGRAPKLL VHGASNLQRGVPSRFSGSGFHTTFTLTISSLQPDDVATYFCAAFQWF GPGTKVEIKRT 456 12a20kc DIQMTQSPSSLSASVGDRVSIHCQAGQGIGSSLNWYQQKPGRAPRLL VHGASNLQRGVPSRFSGSGFHTTFTLTISSLQPDDVATYWCAALEFFG PGTKVEI 457 12a21kc DIQMTQSPSSLSASVGDRVTINCQAGQGIGSSLNWYQKKPGRAPKLL VHGASNLQRGVPSRFSGSGFHTTFTLTISSLQPDDVATYFCAVFQWF GPGTKVDIKRTVAAPSVFIFPPSDEQLK 458 12a22kc DIQMTQSPSSLSASVGDRVTITCQAGQGIGSSLNWYQQKPGRAPKLL VYGASNLQRGVPSRFSGSGFHTTFTLTISSLQPEDFATYFCSVYEFLG PGTKVEIKRTVAAPSVFIFPPSDEQ 459 12a23kc DIQMTQSPSSLSVSVGDRVSITCRATQGIGNSLNWYQQKPGKAPKVLI YGTTKLHGGVPSRFSGGGSGSTGTLTIDSLQPEDIATYFCQLFEFFGP GTKVEIKRTVAAPSVFIFPPSDEQ 460 12a27kc DIQMTQSPSSLSASVGDRVTITCQASQGIGSSLQWYQQKPGRAPNLL VHGASNLHRGVPSRFSGSGFHTTFSLTISGLQRDDFATYFCAVLEFFG PGTKVDIKRTVAAPSVFIFPPSDEQ 461 12a46kc DIQMTQSPSSLPASVGDTVTITCQAGQGIGSSLQWYQQRPGRAPNLL VYDASNLQRGVPSRFTGTGFHTTFTLTIRGLRPEDFGTYFCASLEFFG PGTKVDIKRTVAAPSVFIFPPSDEQ 462 12a55kc YIQMTQSPSSLSASIGDRVTITCQAGQGIGSSLNWYQQKPGKAPKLLV HGASNLQRGVSSRFSGSGFHTTFTLTISSLRPEDVGTYFCEVYEFIGP GTKVDIKRTVAAPS VFIFPPSD EQ 463 12a56kc DIQMTQSPSSLSASVGDRVSINCQAGQGIGSSLNWYQQKRGKAPKLL VHGASTLQRGVPSRFSGSGFHTTFTLTISSLQPDDVATYFCESFQWFG PGTKVEIKRTVAAPSVFIFPPSDEQ 464 12a6kc DIQMTQSPSSLSASVGDRVTITCQASQGIGSSLQWYQQKPGRAPKLLV HGASNLHRGVPSRFSGSGFHTSFTLTISSLQPDDVATYFCAVLEFFGP GTKVEIKRTVAAPSVFIFPPSDEQ 465 12a7kc DIQMTQSPSSLSASVGDRVSIHCQAGQGIGSSLKWYQQKSGRAPRLL VHGASNLQRGVPSRFSGSGFHTTFTLTISSLQPDDVATYWCAVLEFFG PGTKVEIKRTVAAPSVFIFPPSDEQ 466 LSSB2339LC QSVLTQPPSASGAPGQRVTISCSGGPSNVGGNYVYWYRQFPGTAPN LLILRDDQRPSGVPDRFSASKSGNSASLAISGLRPDDEAFYFCATYDS DGSVRLFGGGTTLTVLSQPKAAPSVTLFPPSNGGR 467 LSSB2351LC QSALTQTPSVSGAPGQRVTISCSGGPSNVGGNYVYWYQQFPGAAPK LLIRRDDQRPSGVPDRFSGSKSGNSASLAISGLRLDDEAYYFCATYDS GWSIRLFGGGTRLTVLSQPKAAPSVTLFPPSSEEL 468 LSSB2364LC SQAWTQPPSVSGAPGQRVTISCSGGPSNVGGNLVYWYKQFPGTAP KLLIRRDDQRPSGVPDRFSGSKSGNSASLAISGLRPDDEAFYFCATYD SHGSIRLFGGGTLLTVLSQPKAAPSVTLFPP 469 LSSB2367LC QTVVTQPPSASGTPGQRVTISCSGGGSNIGGNLVSWYQHFPGAAPKL LIYRNDQRPSGVPDRFSGSKSGTSASLTISGLRSDDEATYFCAAYDCT LSLRLFGGGTTLNVLSQPKAAPSVTLFPPSSEEL 470 LSSB2490LC QSALTQPPSVSGTPGQNVTISCSGGGSNVGGNLVSWYQHFPGAAPK LLIHRDNQRPSGVPDRFSVLKSGNSASLAISGPRSDDEAFYFCAVYDS SLSLGLFGGGTKLTVLSQPKAAPSVTLFPPSSEEL 471 LSSB2530LC QSALTQPPSASGAPGQRVTISCSGGPSNVGGNYVYWYRQFPGTAPT LLILRDDQRPSGVPDRFSASKSGNSASLAISGLRPDDEGFYFCATYDS DGSIRLFGGGTALTVLSQPKAAPSVTLFPPSSEELK 472 LSSB2554LC NFMLTQAPSASGAPGQRVTISCSGGPSNVGGNYVYWYRQYPGTAPK LLILRDDQRPSGVPDRFSASKSGNSASLAISELRPDDEAFYFCATYDSD GSIRLFGGGTALTVLSQPKAAPSV 473 LSSB2586LC NFMLTQPPSASGAPGQRVTISCSGGPSNVGGNYVYWYRQFPGTAPN LLILRDDQRPSGVPDRFSASKSGNSASLAISGLRPDDEAFYFCATYDS DGSIRLFGGGTTLTVLSQPKAAPSVTLFPP 474 LSSB2612LC QSVLTQPPSASGAPGQRVTISCSGGPSNVGGNYVYWYRQFPGTAPK LLILRDDQRPSGVPDRFSASKSGNSASLAISGLRPDDEAFYFCATYDS DGSIRLFGGGTALTVLSQPKAAPS 475 LSSB2640LC QLVLTQPPSVSGTPGQNVTISCSGGGSHVGGNLVSWYQHFPGAAPKL LIHRDNQRPSGVPDRFSALKSGNSASLAISGLRSDDEAFYFCAVYDSS LSLGLFGGGTKLTVLSQPKAAPSVT 476 LSSB2644LC RTVVTQPPSVSGAPGQRVTISCTGSSSNIGAGYDVHWYQQLPGTAPK LLIYGNSNRPSGVPDRFSGSKSGTSASLAITGLQAEDEADYYCQSYDS SLSGSGVFGTGTKVTVLGQPKANPTVTLFPPSSEEL 477 LSSB2666LC QSALTQPPSASGAPGQRVTISCSGGPSNVGGNYVYWYRQFPGTAPK LLILRDDQRPSGVPDRFSASKSGNSASLAISGLRPDDEALYFCATYDS DGSIRLFGGGTALTVLSQPKAAPSVTLFPPGWEE 478 LSSB2680LC QPVLTQPPSASGAPGQRVTISCSGGPSNVGGNYVYWYRQFPGTAPN LLILRDDQRPSGVPDRFSASKSGNSASLAITGLRPDDEAFYFCATYDS DGSIRLFGGGTALTVLSQPKAAPSVTLFPP 479 LSSB2683LC QSALTQPPSASGAPGQRVTISCSGGPSNVGGNYVYWYRQFPGTAPN LLILRDDQRPSGVPDRFSASKSGNSASLAISGLRPDDEAFYFCATYDS DGSIRLFGGGTTLTVLSQPKAAPSVTLF 480 LSSB344LC QSALTQTPSVSGAPGQRVTISCSGGPSNVGGNYVYWYQQFPGAAPK LLIRRDDQRPSGVPDRFSGSKSGNSASLAISGLRLDDEAYYFCATYDS GWSIRLFGGGTRLTVLSQPKAAPSVTLFPPSSEEL 481 LSSNEC107LC QLVLTQPPSVSATPGQTVTISCSGSGSNVGGNHVYWYRQLPGAAPTL VISKTDHRPSRVPDRFSGSKSGNSASLAISGLRPDDEAAYFCATYDTG LSLRLFGGGTRLAVLSQPKAAPSVTLFPPSSEEL 482 LSSNEC108LC QSALTQPPATSGTPGQRVTISCSGGGSNVGGNLVSWYQQFPGAAPK LILHRDGQRPSGVPDRFSASKSGTSASLTISGLRSDDEATYFCAAFDS ALSLPLFGGGTKLTVLSQPKAAPSVTLFPPSSEEL 483 LSSNEC117LC QSVLTQVLSVSGTPGQRVIISCSGTSSNVGGNLVSWYQHLPGAAPRLL IHRDDQRPSGVPDRFSGSKSGNSASLVISGLRSDDEADYFCGAYDST FSLPVFGGGTRLTVLSQPKAAPSVTLFPPSSEEL 484 LSSNEC118LC NFMLTQPPSVSATPGQTVTISCSGSGSNVGGNHVYWYRQLPGAAPTL VISKTDHRPSRVPDRFSGSKSGNSASLAISGLRPDDEAVYFCATYDTG LSLRLFGGGTRLTVLSQPKAAPSVTQFPPSSEE 485 LSSNEC122LC QSALTQPPSVSATPGQTVTISCSGSGSNVGGNHVYWYRQLPGAAPTL LISKTNHRPSQVPDRFSASKSGNSASLAISGLRPDDEADYFCGTYDTS LSLRLFGGGTRLTVLSQPKAAPSVTLFPPSSEEL 486 LSSNEC24LC QSALTQPPSASGTPGQRVTISCSGGGSNIGGNLVSWYQHFPGTAPKL LIYRNDQRPSGVPDRFSGSKSGTSASLTISGLRSDDEATYFCAAYDSS LSLRLFGGGTTLNVLSQPKAAPSVTLFPPSSEEL 487 LSSNEC2LC QSALTQPPSVSGTPGQNVTISCSGGGSDVGGNLVSWYQHFPGAAPK LLIHRDNQRPSGVPDRFSALKSGNSASLAISGLRSDDEAFYFCAVYDS SLSLGLFGGGTKLTVLSQPKAAPSVTLFPPSSEEL 488 LSSNEC33LC QAVVTQPPSVSATPGQTVTISCSGSGSNVGGNHVYWYRQLPGAAPTL LISKTNRRPSQVPDRFSGSKSGNSASLAISGLRPDDEADYFCATYDTD LSLRLFGGGTRLTVLSQPKAAPSVTLFPPSSEEL 489 LSSNEC46LC QSALTQPPAASGAPGQRVTISCSGGGSNVGGNLVSWYQQFPGAAPK LILHRDGQRPSGVPDRFSASKSGTSASLTISGLRSDDEATYFCAAYDS AVSLPVFGGGTKLTVLSQPKAAPLVT 490 LSSNEC48LC NFMLTQPPSASGTPGQRVTISCSGGGSNIGGNLVSWYQHFPGAAPKL LIYRNDQRPSGVPDRFSGSKSGTSASLAISGLRSDDKATYFCAAYDST LSLRLFGGGTTLTVLSQPKAAPSVTLFPPSSEE 491 LSSNEC52LC QSVLTQVLSVSGTPGQRVIISCSGTSSNVGGNLVSWYQHLPGAAPRLL IHRDDQRPSGVPDRFSGSKSGNSASLVISGLRSDDEADYFCAAYDSTF SLPVFGGGTRLTVLSQPKAAPSVTLFPPSSE 492 LSSNEC56LC QSALTQPPSVSATPGQTVTISCSGSGSNVGGNHVYWYRQLPGAAPTL LISKTDHRPSRVPDRFSASKSGNSASLAISGLRPDDEAIYFCATYDTGL SLRLFGGGTRLTVLSQPKAAPSVTLFPPSSEEL 493 LSSNEC60LC QSALTRTPSVSGAPGQRVTISCSGGPSNVGGNYVYWYQQFPGAAPK LLIRRDDQRPSGVPDRFSGSKSGNSASLAISGLRLDDEAYYFCATYDS GWSIRLFGGGTRLTVLSQPKAAPSVTLFPPSSEEL 494 LSSNEC70LC QSALTQAPSASGTPGQRVTISCSGGGSNIGGNLVSWYQHFPGAAPKL LIYRNDQRPSGVPDRFSASKSGTSASLAISGLRSDDEATYFCAAYDST LSLRLFGGGTTLAVLSQPKA 495 LSSNEC72LC NFMLTQPPSVSGAPGQRVTISCSGGPSNVGGNLVYWYKQFPGTAPKL LIRRDDQRPSGVPDRFSGSKSGNSASLAISGLRPDDEAFYFCATYDSH GSIRLFGGGTLLTVLSQPKAAPSVTLFPPSSEEL 496 LSSNEC7LC QLVLTQPPSVSGAPGQRVTISCSGGPSNVGGNLVYWYKQFPGTAPKL LIRRDDQRPSGVPDRFSGSKSGNSASLTISGLRPDDEAFYFCATYDSQ GSTRLFGGGTVLTVLSQPKAAPSVTLFPPSSEEL 497 LSSNEC89LC QSALTQPPSVSGAPGQRVTISCSGGPSNVGGNYVYWYRQFPGTAPK LLILRDDQRPSGVPDRFSASKSGNSASLAISGLRPDDEAFYFCATYDS QGSFRVFGGGTALTVLSQPKAAPSVTLYPPSSEE 498 LSSNEC94LC NFMLTQPPSASGAPGQRVTISCSGGPSNVGGNYVYWYRQFPGTAPN LLILRDDQRPSGVPDRFSASKSGNSASLAISGLRPDDEAFYFCATYDS DGSIRLFGGGTTLTVLSQPKAAPSVTLFPPSSEEL 499 LSSNEC9LC QVLSVSGTPGQRVIISCSGTSSNVGGNLVSWYQHLPGAAPRLLIHRDD QRPSGVPDRFSGSKSGNSASLVISGLRSDDEADYFCAAYDSTFSLPVF GGGTRLTVLSQPKAAPSVTLYAPSSEE 500 LSSB2066KC PVTLSASVGDRVTITCRASEDISKYLNWYQHKPGKAPKLLIYTASSLET GVPSRFSGSGSGTDFSLTISSLQPDDFATYYCQQSYTSSVTFGQGTR VEVKRTVAAPSVFIFPPSDEQ 501 LSSB2080KC PATLAVSPGERATISCKSSQNLLYSANNQHSLAWYQQRPGQPPKLLLY WASTRLSGVPDRFSGSGSGTDFTLTISNLQAEDVAVYYCQQYYSPPP TFGQGTKVEIRRTVAAPSVFIFPPSDEQL 502 LSSB2133KC TLSASVGDRVTITCRASQSINNYLNWYQQKPGKAPKLLIYAASSLQSG VPSRFSGSGSGTDFTLTISSLQPEDFVTYYCQQTYSNPRMFGQGTKV EIKRTVAAPSVFIFPPSDEQ 503 LSSB2182KC KAPATLSLSPGERATLSCRASQSVGSDLAWYQQKPGQAPRLLIYDAS NRATAIPARFSGSGSGTDFTLSISSLEPEDFAVYFCQQRYDKITFGQGT RLEIQRTVAAPSVFIFPPSDEQ 504 LSSB331KC RGPVTLAVSLGERATITCKSSQSVLVHSNNKNYLSWYQQKPGQPPKL LIYWASTRESGVPERFSGSGSGTDFTLSISSLQAEDVAVYYCHQYFST PRTFGQGTKVEIKGTVAAPSVFIFPPSDEQL 505 3A124KC SEIVLTQSPATLSLSPGESATLSCRASQSLSSSLAWYQQKPGQAPRLLI YDTSDRATGIPARFSGRGSGTDFTLTISSLEPEDFAVYYCQQRSNWAI TFGQGTRLEIKRTVAAPSVFIFPPSD 506 3A125KC EIVLTQSPGTLSLSPGEXATLSCRASQTISNNYLXWYQQKAGQAPRLLI YGASSGATGIPDRFSGSGSGTDFTLTISRLEPEDFAVYYCQQYGLSPW TFGRGTKVEIKRTVAAPSVFIFPPSD 507 3A140LC QSALTQPRSVSGSPGQSVTISCTGTSSDVGAYNYVSWYRQHPGKAP KLMINDVSKRPSGVPDRFSGSKSGNTASLTISGLQAEDEADYYCCSYA GTYSYVFGTGTKVTVLGQPKANPTVTLFPPSSEEL 508 3A144KC APVTLSASVGDTVTITCRASQPIATFLNWYQHKPGQAPKLLIYAASTFQ RGAPSRYSGSGSGTDFTLTINSLQPEDLATYYCQQTFTDPVTFGQGT RLEIKRTVAAPSVFIFPPSD 509 3A160KC DIQMTQSPASLSASVGDRVTITCRASQGISHYLAWYQQKPGKVPRLLI YAASRLQSGVTSRFSGSGSGTEFTLTISSLLPEDAAVYFCQKYDTDPM TFGQGTRLEIKRTVAAPSVFIFPPSD 510 3A18KC DIQMTQSPSSLSASIGDRVTITCRANQHIRSFLNWYQQTPGKAPKLLIY AASTLQRGVPSRFSGSGSGTDFTLTITSLEREDLATYYCQQTYTSPITF GQGTRLEIKRTVAAPSVFIFPPSDE 511 3A204KC EIVLTQSPGTLSLSPGERATLSCRASQSVSNNYLAWYQQKPGQAPRLL IYGASSRATGIPDRFSGSGSGTDFTLTISRLEPEDFAVYYCQQYATSSL YTFGQGTKLEIKRTVAAPSVFIFPPSD 512 3A228KC LSVSLGERATINCKSSQSILYSSDKKNYLAWYQQKIGQPPKLLLYWAST RESGIPDRFSGSGSGSDFTLTISSLQPEDVAVYYCQQYYISPFTFGPGT KVDLKRTVAAPSVFIFPPSD 513 3A233LC NFMLTQPASVSGSPGQSITLSCTGTTSDVRDSNFVSWYQQVPGKAPK LIIYDVSARPSGVSFRFSGSKSGNTASLTISGLQAEDEALYYCSSFTPT NTLVFGGGTKLTVLGQPKAAPSVT 514 3A244LC SQSWTQEPSLTVSPGGTVTLTCGPSTGAVTSGFYPHWFQQKPGQA PRALIYSTSNKYSWTPARFSGSLLGGKAVLTLSDVQPDDEAEYYCLLLL YYGGPWIFGGGTKLTVLVS 515 3A255LC QAVVTQEPSLTVSPGGTVTLTCASSTGAVTSGFYPHWFQQKPGQAPR ALIYSTSNRYSWTPARFSGSLLGGKAALTLSGVQPEDEAEYYCLLLPY YGGPWIFGGGTKLTVLGQPKAAPSVTLFPPSSEEL 516 3A296KC EIVMTQSPATLSVSPGDRATLSCRASQSVSTNLAWYQQKPGQAPRLLI YGASTRATGIPATFSGSGFATEFTLTISSLQSEDFAVYYCQQYNNWPP AFGQGTKVEIKRTVAAPSVFIFPPSD 517 3A334LC QSVLTQPPSASGSPGQSITISCTGTSSDVGGYNYVSWYQQPPGKAPK VIIYEVSKRPSGVPDRFSGSKSGNTASLTVSGLQAEDEADYYCSSYAG SNNFVFGTGTEVTVVGQPKANPTVTLFPPSSEELL 518 3A366KC SLSASVGDRVTITCRASESISFYLNWYQQKPGKAPELLIFATSTLHSGV PSRFSGSGSGTDFTLTISSLQLEDFATYYCQQSSSTPFTFGGGTKVEIK RTVAAPSVFIFPPSD 519 3A384KC DIQMTQSPSSLSAYVGDRVTITCRASQNINTYLNWYQQRPGKAPKLLIY AASTLQSGVPSRFSGSGSGTDFTLTISNLETEDFAVYYCQQTYRSVTF GQGTKLEIKRTVAAPSVFIFPPSD 520 3A419KC LSAYVGDRVTITCRASQNINTYLNWYQQRPGKAPKLLIYAASTLQSGV PSRFSGSGSGTDFTLTISNLETEDFAVYYCQQTYSSVTFGQGTKLETR RTVAAPSVFIFPPSD 521 3A461KC SEIVLTQSPGTLSLSPGERATLSCRASQSVSSSYLAWYQQKPVQAPRL LIYGASSRATGIPDRFSGSGSGTDFTLTISRLEPEDFAVYYCQQYGTLH PRTFGQGTKVEIKRTVAAPSVFIFPPSD 522 3A474KC EIVLTQSPGTLSLSPGERATLSCRASQSISSNYLAWYQQKPGQAPRLLI YGASTRATGIPDRFSGSGSGTDFTLSISRLEPEDIAVYYCHQYGSSQR FGQGTKVEIKRTVAAPSVFIFPPSD 523 3A518KC DIQMTQSPSSLSASVGDRVTITCRASQSISRYLNWYQQKPGKAPKLLIY AASSLQGGVPSRFSGSGSGTDFTLTISSLQPEDFATYYCQQSSSKPFT FGGGTKVEIKRTVAAPSVFIFPPSD 524 3A539LC NFMLTQPASVSGSPGQSITISCSGTGSDIGVYNYVSWYQQHPGKAPR LMIYDVTNRPSGVSNRFSGSKSGFTASLTISGLQGDDEADYYCSSYSS TNTYVFGTGTHVTVLGQPKANPTVTLFPPSSEEL 525 3A576LC QSALTQPPSASGTPGQRVTISCSGSYHNIGSNAVNWYQQLPGTAPKL LIYSNDQRPSGVPDRFSGSKSGTSASLAISGLQSEDEADYYCAAWDD SLHVFGTGTKVTVLGQPKANPTVTLFPPSSEEL 526 3A613LC QSALTQPPSASGTPGQRVTISCSGSYHNIGSNAVNWYQQLPGTAPKL LIYSNDQRPSGVPDRFSGSKSGTSASLAISGLQSEDEADYYCAAWDD SLHVFGTGTKVTVLGQPKANPTVTLFPPSSEEL 527 3A64KC DIQMTQSPSSLSASVGDRVTITCRASQDITTYLAWLQQKPGKAPKSLIY SASTVQSGVPSRFSGSGSGTEFTLTISGLQPEDFATYYCQQYNYYPIT FGLGTRLEIKRTVAAPSVFIFPPSDE 528 3A650KC IILFLVATATGSWAQSALTQPRSVSGSLGQSVTISCTGSSSDVGRYNYV SWYQHHPGKAPKLMISDVNKRPSGVPDRFSGSKSGNTASLTISGLQA EDETDYYCCSYAGSYIWVFGG 529 3A67KC EIVLTQSPATLSLSPGERATLSCRASQSVSSYLAWYQQKPGQAPRLLI YDASNRATGIPARFSGSGSDTDFTLTISSLEPEDFAVYYCQQRGIWPL QITFGQGTRLEIKRTVAAPSVFIFPPSDE 530 3A779KC LSASVGDRVTITCRASQSIDRYLNWYQQKPGKAPKLLIYAASSLHTDVP SRFSGSGAGTYFTLTITSLQPEDFATYYCQQSHSPSFGQESYSITFGQ GTRLEIKRTVAAPSVFIFPPSD 531 3A816KC VTLSLSPGERATLSCRASQTISNNYLAWYQQKPGQAPRLLIYGASSGA TGLPDRFSGSGSGTDFTLTISRLEPEDFAVYYCHQYALSPWTFGRGTK VEIKRTVAAPSVFIFPPSD 532 3A869KC IILFLVATATGVHSDIQMTQSPSSLSASVGDRVTITCRASQSIDRYLNWY QHKPGKAPKLLIYAASNLHTDVPSRFSGSGAGTYFTLTITSLQPEDFAT YYCQQSHSPSFGQESYSIAFGQGTRLEIKRTVAAPSVFIFPPSDE 533 3A93LC QSVLTQPASVSGSPGQSITISCTGTNSDVGYSYVSWFQQHPGKVPKL LIYDVSRRSSGVSNRFSGSRSGNTASLTISGLRAEDEADYYCGSFTTS LTLVFGGGTKLAVLVSPS 534 3a426kc EIVLTQSPGTLSLSPGERATLSCRASQSVSSRYLAWYQQKPGQAPRLII YDASSRASGIPDRFSGSGSETDFTLTITRLEPEDFAVYYCQLYGTSPKF TFGQGTKLEIKRTVAAPSVFIFPPSD 535 3a515kc DVVMTQSPLSLPVTLGQPASISCRSSQSLVYSHGDTYLKCFQQRPGQ SPRRPIYKVSNRDSGVPDRFSGSGSGTDFTLKISRVEAEDVGV 536 3b129kc GPATLSVSPGERATLSCRASQSLRNNLAWYQQKTGQSPRLLIYAVST RATGIPPRFSGGGSGTEFTLTIDSLQSEDFAVYFCQQYDSPQWTFGQ GTKVEIKRTVAAPSVFIFPPSD 537 3b171lc QSVLTQPASVSGSPGQSITISCTGTSNDVGGQNFVSWYQQHPGTAPQ LLIYDVTNRPAGVSSRFSGSKSGNTASLTISGLRTEDEADYYCASFTIL NGVDYVFGTGTKVTVLLSPSQPYL 538 3b27kc EIVLTQSPATLSVSPGERATLSCRAGQSVSSDLAWYQHKPGQAPRLLI YDASKRATGIPARFSGSGSGTDFTLTISSLEPEDFAVYYCQHRTNWPP SITFGQGTRLEIKRTVAAPSVFIFPPSD 539 3b41kc EIVLTQSPGTLSLSPGERATLSCRASQSVSSNYLAWYQQKPGQAPRLL IYGASSRATGIPDRFSGSGSGTDFTLSISRLEPEDFAVYYCQQYGTSS CTFGQGTKLEIKRTVAAPSVFIF 540 3b45kc EIVLTQSPGTLSLSPGDRAALSCRASETLSGNSLAWYQQKRGQPPRLL IFAASSRATGIPERFSGGGSGTDFTLTITRLEPEDFAVYFCQQYVDAPIT FGQGTRLEIKRTVAAPSVFIFPPSD 541 3b46kc EIVLTQSPGTLSLSPGERATLSCRASQSVSSNNLAWYQQKPGQAPRLL MSGASSRATGIPDRFSGSGSGTDFTLTISRLEPEDFAVYHCQQYGSSP PTFGQGTKVEIKRTVAAPSVFIFPP 542 3b57lc QSVLTQPRSVSGSPGQSVTISCTGTSSDVGGYNYVSWYQQHPGKAP KTMIFDVTKRPSGVPDRFSGSKSGNTASLTISGLQAEDEADYYCSSYA GRNTFYVFGTGTTVTVQVSPSQPPP 543 3b8kc EIVLTQSPGTLSLSPGERATLSCRASQSVSSNLAWYAQKPGQAPRLIIY GASSRASAIPDRFRGSGSGTDFTLTISRLEPEDFAVYYCQQYDDAPITF GHGTRLEIKRTVAAPSVFIFPPSDE 544 3BNC55KC DIQMTQSPSSLSASVGDKVTITCQTSAGYLNWYQQRRGRAPKLLMYD GSRLVTGVPSRFSGRRWGTQYNLTIGSLQPEDIATYYCQVYEFFGPG TRLDLKSTVAA 545 3BNC60KC DIQMTQSPSSLSARVGDTVTITCQANGYLNWYQQRRGKAPKLLIYDGS KLERGVPARFSGRRWGQEYNLTINNLQPEDVATYFCQVYEFIVPGTRL DLKRTVAA 546 3anc3kc DIQMTQSPSSVSASVGDRVTITCQASRDTDNSLTWYQQKPGRPPKLLI YHVVNLGPGVPSRFSGSASSATQSTLIISDFQPDDVATYFCQNYEFFG PGTKVEIKRTVAAPSVFIFPPSDEQ 547 3b106kc DIQMTQSPSSLSASVGDTVTITCQANGYLNWYQQRRGKAPKLLIYDGS KLERGVPSRFSGRRWGQEYNLTINNLQPEDIATYFCQVYEFVVPGTRL DLKRTVAAPSVFIFPPSD 548 3b16kc DIQMTQSPSSLSASVGDTVTITCQANGYLNWYQQRRGKAPKLLIYDGS KLERGVPSRFSGRRWGQEYNLTINNLQPEDIATYFCQVYEFVVPGTRL DLKRTVAAPSVFIFPPSD 549 3b180kc DIQMTQSPSSLSARVGDTVTFTCQANGYLNWYQQRRGKAPKLLIYDG SKLERGVPSRFSGRGWGQEYNLTINNLQPEDIATYFCQVYEFAVPGT RLDLKRTVAAPSVFIFPPSD 550 3b183kc DIQMTQSPSSLSARVGDTVTITCQANGYLNWYQQRRGKAPKLLIYDGS KLETGVPSRFTGRRWGQEYNLTINNLQPEDIATYFCQVYEFIVPGTRL DLKRTVAAPSVFIFPPSD 551 3b191kc DIQMTHSPSSLSASVGDTVTITCQANGYLNWYQQRRGKAPKLLIYDGS KLETGVPSRFTGRRWGQEYNLTINNLQPEDIATYFCQVYEFIVPGTRL DLKRTVAAPSVFIFPPSD 552 3b21kc DIQMTQSPSSLSARVGDTVTITCQANGYLNWYQQRRGKAPKLLIYDGS KLETGVPSRFTGRRWGQEYNLTINNLQPEDIATYFCQVYEFIVPGTRL DLKRTVAAPSVFIFPPSD 553 3bnc102kc DIQMTQSPSSLSASVGDRVTITCQASQGISNSLNWYQQKPGKAPRLLI YGTSTLQRGVPSRFSGSGSGTRFTVTINSLQPEDIATYFCQHNEFFGR GTKVDIKRTVAAPS VFIFPPSD EQL 554 3bnc104kc DIQMTQSPSSLSASIGDRVNITCQASRDTGSALNWYQQKVGRPPRLLI SAVSNLGAGVPSRFSGRRSGTQSTLTINTLQPEDIATYFCQHYEFFGP GTKVDIKRTVAAPSVFIFPPSDEQ 555 3bnc105kc DIQMTQSPSSLSASVGDTVTFTCQANGYLNWYQQRRGKAPKLLIYDG SRLERGVPSRFSGRRWGQEYNLTINNLQPEDIATYFCQVYEFAVPGT RLDLKRTVAAPSVFIFPPSD 556 3bnc107kc DIQMTQSPSSLSASVGDTVTITCQTNKGYLNWYQQRRGRAPKLLMYD GSKLVTGVPSRFSGRRWGTQYNLTIGSLQPEDIATYYCQVYEFFGPGT RLDLKRTVAAPSVFIFPPSD 557 3bnc108kc DIQMTQSPSSLSARVGDKVTITYQTSAGYLNWYQQRRGRAPKLLMYD GSRLVTGAPSRFSGRRWGTQYNLTIGSLQPEDIATYYCQVYEFFGPG TRLDLKRTVAAPSVFIFPPSD 558 3bnc117kc DIQMTQSPSSLSASVGDTVTITCQANGYLNWYQQRRGKAPKLLIYDGS KLERGVPSRFSGRRWGQEYNLTINNLQPEDIATYFCQVYEFVVPGTRL DLKRTVAAPSVFIFPPSD 559 3bnc134kc DIQMTQSPSSLSASVGDTVTINCQTNKGYLNWYQQRRGRAPKLLMYD GSKLVTGVPSRFSGRRWGTQYNLTIGSLQPEDIATYYCQVYEFFGPGT RLDLKRTVAAPSVFIFPPSD 560 3bnc142kc DIQMTQSPSSLSASVGDTVTITCHTNKGYLNWYQQRRGRAPKLLMFD GSKLVTGVPSRFSGRRWGTQYNLTIGSLQPEDIATYYCQVYEVFGPG TRLDLKRTVAAPSVFIFPPSD 561 3bnc151kc DIQMTQSPSSLSASVGDTVTITCQTNKGYLNWYQQRRGRAPKLLMYD GSKLVTGVPSRFSGRRWGTQYNLTIGSLQPEDIATYYCQVYEFFGPGT RLDLKRTVAAPSVFIFPPSD 562 3bnc153kc DIQMTQSPSSLSASVGDTVTITCQTNKGYLNWYQQRRGRAPKLLMYD GSKLVTGVPSRLSGRRWGTQYNLTIGSLQPEDIATYYCQVYEFFGPGT RLDLKRTVAAPSVFIFPPSD 563 3bnc156kc DIQMTQSPSSLSASVGDTVTITCQTNKGYLNWYQQKRGRAPKLLMYD GSKLVTGVPSRLSGRRWGTQYNLTIGSLQPEDIATYYCQVYEFFGPGT RLDLKRTVAAPSVFIFPPSD 564 3bnc158kc DIQMTQSPSSLSASVGDTVTITCQTNKGYLNWYQQRRGRAPKLLMYD GSKLVTGVPSRLSGRRWGTQYNLTIGSLQPEDIATYYCQVYEFFGPGT RLDLKRTVAAPSVFIFPPSD 565 3bnc159kc DIQMTQSPSSLSASVGDTVTITCQTNKGYLNWYQQRRGRAPKLLMYD GSKLVTGVPSRFSGRRWGTQYNLTIGSLQPEDIATYYCQVYEFFGPGT RLDLKRTVAAPSVFIFPPSD 566 3bnc15kc DIQMTQSPSSLSASVGDTVTITCQTNKGYLNWYQQRRGRAPKLLMYD GSKLVTGVPSRLSGRRWGTQYNLTIGSLQPEDIATYYCQVYEFFGPGT RLDLKRTVAAPSVFIFPPSD 567 3bnc176kc DIQMTQSPSSLSASVGDTVTITCQANGYLNWYQQRRGKAPKLLIYDGS KLERGVPSRFSGRRWGQEYNLTINNLQAEDIATYFCQVYEFAVPGTRL DLKRTVAAPSVFIFPPSD 568 3bnc193kc DIQMTQSPSSLSARVGDKVTITCQTSAGYLNWYQQRRGRAPKLLMYD GSRLVTGVPSRFSGRRWGTQYNLTIGSLQPEDIATYYCQVYEFFGPG TRLDLKRTVAAPSVFIFPPSD 569 3bnc196kc DIQMTQSPSSLSASVGDTVTITCQANGYLNWYQQRRGKAPKLLMYDG STLERGVPARFSGRRWGQEYNLTINNLQPEDVATYFCQVYEFIVPGTR LDLKRTVAAPSVFIFPPSD 570 3bnc31kc DIQMTQSPSSLSASVGDTVTITCQTNKGYLNWYQQRRGRAPKLLMCD GSKLVTGVPSRFSGRRWGTQYNLTIGSLQPEDIATYYCQVYEFFGPGT RLDLKRTVAAPSVFIFPPSD 571 3bnc42kc DIQMTQSPSSLSASVGDTVTITCQTTKGYLNWYQQRRGRAPKLLMFD GSKLVTGVPSRFSGRRWGTQYNLTIGSLQPEDLATYYCQVYEFFGPG TRLDLKRTVAAPSVFIFPPSD 572 3bnc53kc DIQMTQSPSSLSASVGDTVTITCHTNKGYLNWYQQRRGRAPKLLMFD GSKLVTGVPSRFSGRRWGTQYNLTIGSLQPEDIATYYCQVYEVFGPG TRLDLKRTVAAPSVFIFPPSD 573 3bnc62kc DIQMTQSPSSLSARVGDTVTITCQANGYLNWYQQRRGKAPKLLIYDGS KLETGVPSRFTGRRWGQEYNLTINNLQPEDIATYFCQVYEFIVPGTRL DLKRTVAAPSVFIFPPSD 574 3bnc65kc DIQMTQSPSSLSARVGDTVTFTCQANGYLNWYQQRRGKAPKLLIYDG SKLERGVPSRFSGRRWGQEYNLTINNLQPEDIATYFCQVYEFAVPGTR LDLKRTVAAPSVFIFPPSD 575 3bnc66kc DIQMTQSPSSLSASVGDTVTITCQTNKGYLNWYQQRRGRAPKLLMYD GSKLVTGVPSRLSGRRWGTQYNLTIGSLQPEDIATYYCQVYEFFGPGT RLDLKRTVAAPSVFIFPPSD 576 3bnc75kc DIQMTQSPSSLSARVGDTVTITCQANGYLNWYQQRRGKAPKLLIYDGS KLERGVPSRFSGRRWGQEYNLTINNLQPEDIATYFCQVYEFVVPGTRL DLKRTVAAPSVFIFPPSD 577 3bnc79kc DIQMTQSPSSLSARVGDTVTFTCQANGYLNWYQQRRGKAPKLLIYDG SKLERGVPSRFSGRRWGQEYNLTINNLQPEDIATYFCQVYEFAVPGTR LDLKRTVAAPSVFIFPSD 578 3bnc81kc DIQMTQSPSSLSASVGDTVTINCQTNKGYLNWYQQRRGRAPKLLMYD GSKLVTGVPSRFSGRRWGTQYNLTIGSLQPEDIATYYCQVYEFFGPGT RLDLKRTVAAPSD 579 3bnc84kc DIQMTQSPSSLSASVGDTVTINCQTNKGYLNWYQQRRGRAPKLLMYD GSKLVTGVPSRFSGRRWGTQYNLTIGSLQPEDIATYYCQVYEFFGPGT RLDLKRTVAAPSVFIFPPSD 580 3bnc87kc DIQMTQSPSSLSARVGDTVTITCQANGYLNWYQQRRGKAPKLLIYDGS KLERGVPSRFSGRRWGQEYNLTINNLQPEDIATYFCQVYEFVVPGTRL DLKRTVAAPSVFIFPPSD 581 3bnc89kc DIQMTQSPSSLSASVGDKVTITCQTSAGYLNWYQQRRGRAPKLLMYD GSRLVTGVPSRFSGRRWGTQYNLTIGSLQPEDVATYYCQVYEFFGPG TRLDLKRTVAAPSVFIFPPSD 582 3bnc91kc DIQMTQSPSSLSARVGDTVTITCQANGYLNWYQQRRGKAPKLLIYDGS KLERGVPSRFSGRRWGQEYNLTINNLQPEDIATYFCQVYEFAVPGTRL DLKRTVAAPSVFIFPPSD 583 3bnc95kc DIQMTQSPSSLSASVGDTVTITCQANGYLNWYQQRRGKAPKLLIYDGS KLERGVPSRFSGRRWGQEYNLTINNLQPEDIATYFCQVYEFIVPGTRL DLKRTVAAPSVFIFPPSD

TABLE 1 Forward Leader Sequence Primers VH1 LEADER-A ATGGACTGGACCTGGAGGAT SEQ ID NO 591 VH1 LEADER-B ATGGACTGGACCTGGAGCAT SEQ ID NO 592 VH1 LEADER-C ATGGACTGGACCTGGACAAT SEQ ID NO 593 VH1 LEADER-D GGCCTTCTCTTTGTGGTGGC SEQ ID NO 594 VH1 LEADER-E ATGGACTGGACCTGGAGGGT SEQ ID NO 595 VH1 LEADER-F ATGGACTGGATTTGGAGGAT SEQ ID NO 596 VH1 LEADER-G AGGTTCCTCTTTGTGGTGGCAG SEQ ID NO 597 VH3 LEADER-A TAAAAGGTGTCCAGTGT SEQ ID NO 598 VH3 LEADER-B TAAGAGGTGTCCAGTGT SEQ ID NO 599 VH3 LEADER-C TAGAAGGTGTCCAGTGT SEQ ID NO 600 VH3 LEADER-D GCTATTTTTAAAGGTGTCC SEQ ID NO 601 AGTGT VH3 LEADER-E TACAAGGTGTCCAGTGT SEQ ID NO 602 VH3 LEADER-F TTAAAGCTGTCCAGTGT SEQ ID NO 603 VH4 LEADER-A ATGAAACACCTGTGGTTCTTCC SEQ ID NO 604 VH4 LEADER-B ATGAAACACCTGTTTCTT SEQ ID NO 605 VH4 LEADER-C ATGAAGCACCTGTGGTTCTT SEQ ID NO 606 VH4 LEADER-D ATGAAACATCTGTGGTTCTT SEQ ID NO 607 VH5 LEADER-A TTCTCCAAGGAGTCTGT SEQ ID NO 608 VH5 LEADER-B CCTCCACAGTGAGAGTCTG SEQ ID NO 609 VH6 LEADER-A ATGTCTGTCTCCTTCCTCATC SEQ ID NO 610 VH7 LEADER-A GGCAGCAGCAACAGGTGCCCA SEQ ID NO 611 Reverse Constant Region Primers 3′ Cg CH1 GGAAGGTGTGCACGCCGCTGGTC SEQ ID NO 612 (gamma) 3′ IgG (internal) GTTCGGGGAAGTAGTCCTTGAC SEQ ID NO 613

TABLE 2 year CD4+ Virus of year of T copies/ clinical gender clade birth diagnosis cells/ul ml status pt1  male B 1948 1985 354 4722 non progressor pt3  male B 1965 2002 427 880 non progressor pt8  male B 1962 1989 580 <50 elite controller pt12 male ND ND ND ND ND ND

TABLE 3A SEQ ID Ab Name VH D JH (−) CDR3 (aa) NO 3BNC4 1-2 7-27 2/6 3 R H S D Y C D F D V 614 3BNC23 1-2 6-25/3-3 2/6 3 Q R S D F W D F D V 615 3BNC42 1-2 7-27 2/6 3 R H S D Y C D F D V 616 3BNC53 1-2 3-3 2/6 3 R H S D Y C D F D V 617 3BNC55 1-2 3-3/6-19/5-12 2/6 3 R H S D Y C D F D I 618 3BNC62 1-2 6-25/6-13/6-6 2/6 3 Q R S D Y W D F D V 619 3BNC65 1-2 6-25/6-6 2/6 3 Q R S D Y W D F D V 620 3BNC66 1-2 7-27 2/6 3 R H T D Y C D F D V 621 3BNC72 1-2 7-27 2/6 3 R H S D Y C D F D V 622 3BNC79 1-2 6-25/6-6 2/6 3 Q R S D Y W D F D V 623 3BNC81 1-2 7-27 2/6 3 R H S D Y C D F D V 624 3BNC89 1-2 3-3/6-19/5-12 2/6 3 R H S D Y C D F D I 625 3BNC91 1-2 2-21/6-25 2/6 3 R R S D Y C D F D V 626 3BNC95 1-2 6-25/2-8 2/6 3 Q R S D Y W D F D V 627 3BNC105 1-2 6-6/6-25 2/6 3 Q R S D Y W D F D V 628 3BNC107 1-2 7-27/3-3 2/6 3 R H S D Y C D F D V 629 3BNC108 1-2 3-3/6-19/6-25 2/6 3 R H S D Y C D F D I 630 3BNC117 1-2 6-25/2-8 2/6 3 Q R S D Y W D F D V 631 3BNC134 1-2 7-27 2/6 3 R H S D Y C D F D V 632 3BNC142 1-2 3-3 2/6 3 R H S D Y C D F D V 633 3BNC151 1-2 7-27/4-17/3-3 2/6 3 R H S D Y C D L D V 634 3BNC156 1-2 3-3/7-27 2/6 3 R H S D Y C D F D V 635 3BNC159 1-2 7-27 2/6 3 R H S D Y C D F D V 636 3BNC176 1-2 6-25/6-6 2/6 3 Q R S D Y W D F D V 637 3BNC196 1-2 6-25/6-6/6-13 2/6 3 Q R S D Y W D F D V 638 3BNC6 1-2 3-16/1-7 2 1 P L R G G D T W H Y H S 639 3BNC101 1-2 1-7/3-16 2 1 P L R G G D T W H Y H S 640 3BNC102 1-2 3-22/1-26/1-20 2 3 P H S P D D A W S L D V 641 3BNC126 1-2 3-22/1-26/1-20 2 3 P H S P D D A W S L D V 642 3BNC149 1-2 3-22/1-26/1-20 2 3 P H S P D D A W S L D V 643 3ANC3 1-2 2-21/2-15 1/2 1 P R G G R D N W S F H V 644 3ANC42 1-2 ND 2 2 P K S G R D Y W S F D L 645 3BNC3 1-69 5-5/5-18/5-24 3 2 A T G Y S Y G Y L D A F D I 646 3BNC8 1-24 5-24/4-17 4 3 E P R E M G T L T A G F E Y 647 3BNC48 1-69 3-3 4 5 G Q T D L N D D L W S D Y S T 648 P G F D Y 3ANC38 1-69 3-3 4 5 G Q T D L N D D F W S E Y S T 649 P G F D Y 3BNC49 1-69 3-22/6-19/5-12 6 3 G E F D S S G F D Y E S W Y P 650 Y Y M D V 3BNC58 1-24 3-16/3-10 4/5 2 A P R L E L G E L S S G F H Y 651 3BNC78 1-24 4/5 2 A P R L D L G E L S S G F H F 652 3BNC78 1-24 4/5 2 A P R L D L G E L S S G F H F 653 3BNC71 1-24 1-24 4/5 3 D N P L L Q S G E F S S S L D N 654 3BNC71 1-24 1-24 4/5 3 D N P L L Q S G E F S S S L E N 655 3BNC144 1-69 3-9/5-5 4 3 A Q G D I L T E G Y F D Y 656 Mutations Primer Ab Name (+) Length HC Set k/l Vk/l Jk/l (−) 3BNC4 1 10 72 new k 1D-33 3 1 3BNC23 1 10 79 new k 1D-33 3 1 3BNC42 2 10 69 new k 1D-33 3 1 3BNC53 2 10 74 new k 1D-33 3 1 3BNC55 2 10 64 new k 1D-33 1/3 1 3BNC62 1 10 81 new k 1D-33 3 1 3BNC65 1 10 82 new k 1D-33 3 1 3BNC66 2 10 69 new k 1D-33 3 1 3BNC72 1 10 72 new k 1D-33 3 1 3BNC79 1 10 76 new k 1D-33 3 1 3BNC81 2 10 71 new k 1D-33 3 1 3BNC89 2 10 68 new k 1D-33 3 1 3BNC91 2 10 76 new k 1D-33 3 1 3BNC95 1 10 72 new k 1D-33 3 1 3BNC105 1 10 77 new k 1D-33 3 1 3BNC107 2 10 69 new 3BNC108 2 10 62 new k 1D-33 3 1 3BNC117 1 10 72 new k 1D-33 3 1 3BNC134 2 10 71 new k 1D-33 3 1 3BNC142 2 10 72 new k 1D-33 3 1 3BNC151 2 10 69 new k 1D-33 3 1 3BNC156 2 10 72 new k 1D-33 3 1 3BNC159 2 10 71 new k 1D-33 3 1 3BNC176 1 10 72 new k 1D-33 3 1 3BNC196 1 10 78 new k 1D-33 3 1 3BNC6 3 12 55 new k 1D-33 1/3 1 3BNC101 3 12 54 new 3BNC102 1 12 63 new k 1D-33 1/3 1 3BNC126 1 12 65 new 3BNC149 1 2 68 new 3ANC3 3 12 59 new k 1D-33 3 1 3ANC42 2 12 53 new k 1D-33 3 1 3BNC3 0 14 22 new L 1-44 1 2 3BNC8 1 14 21 old k 3-11 2 0 3BNC48 0 20 18 new 3ANC38 0 20 12 new 1 1-47 1/6 2 3BNC49 0 20 23 old k 3-20 3 3BNC58 1 15 16 old k 3-11 2 0 3BNC78 2 15 38 old 3BNC78 2 15 39 old 3BNC71 0 16 22 old k 3-11 5 3BNC71 0 16 17 old k 3-11 5 3BNC144 0 13 15 old k/l 1-44/1-47 1 2 SEQ ID Mutations #of Ab Name CDR3 (aa) NO (+) Length LC Binding NEUT Relatives 3BNC4 Q V Y E F 657 0 5 38 + 7 3BNC23 Q V Y E F 658 0 4 50 CD4BS + 5 3BNC42 Q V Y E F 659 0 5 42 − 1 3BNC53 Q V Y E V 660 0 5 42 + 1 3BNC55 Q V Y E F 661 0 5 32 + 1 3BNC62 Q V Y E F 662 0 5 43 + 4 3BNC65 Q V Y E F 663 0 5 44 ND 1 3BNC66 Q V Y E F 664 0 5 38 + 1 3BNC72 Q V Y E F 665 0 5 38 + 1 3BNC79 Q V Y E F 666 0 5 44 ND 2 3BNC81 Q V Y E F 667 0 5 38 ND 2 3BNC89 Q V Y E F 668 0 5 35 + 1 3BNC91 Q V Y E F 669 0 5 42 + 1 3BNC95 Q V Y E F 670 0 5 39 + 9 3BNC105 Q V Y E F 671 0 5 43 ND 1 3BNC107 ND ND 1 3BNC108 Q V Y E F 672 0 5 38 + 2 3BNC117 Q V Y E F 673 0 5 39 CD4BS + 9 3BNC134 Q V Y E F 674 0 5 38 ND 1 3BNC142 Q V Y E V 675 0 5 42 + 1 3BNC151 Q V Y E F 676 0 5 40 ND 1 3BNC156 Q V Y E F 677 0 5 37 + 1 3BNC159 Q V Y E F 678 0 5 39 ND 1 3BNC176 Q V Y E F 679 0 5 41 + 3 3BNC196 Q V Y E F 680 0 5 43 ND 1 3BNC6 Q H Y E F 681 1 5 44 + 24 3BNC101 ND ND 1 3BNC102 Q H Y E F 682 1 5 34 − 1 3BNC126 ND ND 1 3BNC149 ND ND 1 3ANC3 Q H Y E F 683 0 5 47 + 1 3ANC42 Q Q Y E F 684 1 5 41 ND 4 3BNC3 A A W D D T 685 0 9 19 CD4i + 7 L Y V 3BNC8 Q H R S I W 686 2 11 10 CD4i + 3 P L M C T 3BNC48 ND ND 3ANC38 G A W D D 687 0 9 8 CD4i − 2 T L Y V 3BNC49 ND CD4i ND 2 3BNC58 Q Q R T I W 880 1 11 10 CD4i ND 2 P P G C S 3BNC78 ND ND 1 3BNC78 ND ND 2 3BNC71 ND CD4i ND 1 3BNC71 CD4i ND 1 3BNC144 ND 1 9 CD4i ND 1

TABLE 3b Ab SEQ ID Name VH D JH (−) CDR3 (aa) NO 1NC2 1-46 3-22/5-5 4/5 4 N E A D Y H D G N G H S L R G M F D Y 881 1NC3 1-46 6-19 4/5 3 A E A E S Q S H S R P I M F D F 688 1NC7 1-46 6-19/1-14 4/5 3 A E A E S Q S H S R P I M F D S 689 1NC9 1-46 5-12/2-8 4/5 4 Q D S D F H D G H G H T L R G M F D S 690 1NC18 1-46 1-14/2-21 4/5 2 N E P Q Y H S L P G M F D Y 691 1NC24 1-46 3-16 4/5 3 N E P Q Y H D G N G H S L P G M F D Y 692 1NC29 1-46 3-16/6-19 4/5 3 N E P Q Y Y D G S G H S L P G M F D Y 693 1NC33 1-46 5-12 4/5 5 L E A D G D D Y S P K M V D Y 694 1NC46 1-46 3-9/3-16 4/5 3 R E A D Y H D G N G H T L P G M F D F 695 1NC48 1-46 3-9/6-19 4/5 2 N E P Q Y F D G S G H S L P G M F D Y 696 1NC52 1-46 3-16/6-19 4/5 3 N E P Q Y Y D G S G H S L P G M F D Y 697 1NC56 1-46 5-12/3-9 4/5 5 L E A D G D D Y S P K M F D H 698 1NC60 1-46 3-22/1-26 1/5 4 L E A E S D S H S R P I M F D H 699 1NC66 1-46 3-16 4/5 2 N E P Q Y H D G N G H S L P G M F D F 700 1NC70 1-46 3-16/6-19 4/5 3 N E P Q Y Y D G S G H S L P G M F D Y 701 1NC72 1-46 6-19/1-14 4/5 3 A E A E S Q S H S R P I M F D F 702 1NC94 1-46 6-13/6-19 4/5 3 A E A A S D S H S R P I M F D H 703 1NC95 1-46 3-16/6-19 4/5 4 L E A D G S D Y S P K M F D F 704 1NC107 1-46 3-3/5-12 4/5 5 L E A D G D D Y S P K M F D Y 705 1NC108 1-46 3-9/3-16 4/5 4 R E A D Y H D G N G H T L P G M F D F 706 1NC109 1-46 5-1/6-19 4/5 5 L E A D G D D Y S P K M F D Y 707 1NC110 1-46 5-24/6-19 4/5 4 L E A D G D N Y S P K M V D Y 708 1NC116 1-46 2-21 4 2 N E P Q Y H S L P G M F D Y 709 1NC118 1-46 3-9/5-12 4 3 L E A D G G D Y S P K M F D Y 710 1NC122 1-46 3-16/3-3 4 4 L E A D G A D Y S P K M F D F 711 1NC123 1-46 6-19 4 3 A E A E S Q S H S R P I M F D Y 712 1NC127 1-46 6-13/6-19 4/5 3 A E A A S D S H S R P I M F D H 713 1B344 1-46 3-22/1-26 1/5 4 L E A E S D S H S R P I M F D H 714 1B2416 1-46 1-14/3-16 4 4 N E P Q Y H D D N G H S L P G M I D Y 715 1B2503 1-46 6-19 5 3 A E A E S Q S H S R P I M F D S 716 1B2573 1-46 3-22 4/5 2 N E P Q Y H D G N G H S L P G M F D S 717 1NC5 1-69 3-3 3 1 G R Q T F R A I W S G P P V V F D I 718 1NC126 1-69 3-3 3 1 G R Q T F R A I W S G P P A V F D I 719 1NC16 4-34 3-10 5 2 A V A G L W F E D A Y N W F G P 720 1NC21 4-34 3-10 5 2 A V K G L W F D E T Y T W F G P 721 1NC54 4-34 3-10 5 2 A V K G F W F D E P S T W F G P 722 1NC57 4-34 3-10 5 2 A V K G F W F D D P Y T W F G P 723 1NC115 4-34 3-10 5 2 A V K G F W F D E V Y N W F G P 724 Ab Mutations Name (+) Length HC Primer Set k/l Vk/l Jk/l (−) 1NC2 2 19 74 new l 1-47 3 1 1NC3 2 16 86 NEW l 1-47 6/7 1 1NC7 2 16 77 new l 1-47 6/7 1 1NC9 4 19 67 new l 1-47 3 1 1NC18 1 14 85 new 1NC24 2 19 79 new l 1-47 3 1 1NC29 1 19 87 new 1NC33 0 15 84 new l 1-47 3 2 1NC46 3 19 85 new l 1-47 3 1 1NC48 1 19 88 new l 1-47 3 1 1NC52 1 19 82 new l 1-47 3 1 1NC56 2 15 91 new l 1-47 3 1 1NC60 3 16 72 new l 1-47 3 1 1NC66 2 19 91 new l 1-47 3 1 1NC70 1 19 85 new l 1-47 3 1 1NC72 2 16 77 new l 1-47 6/7 1 1NC94 3 16 81 new l 1-47 3 2 1NC95 0 15 93 new 1NC107 1 15 90 new l 1-47 3 1 1NC108 3 19 85 new l 1-47 3 1 1NC109 1 15 85 new 1NC110 1 15 88 new 1NC116 1 14 83 new 1NC118 0 15 86 new l 1-47 3 1 1NC122 1 15 94 new l 1-47 3 1 1NC123 2 16 78 new l 1-47 3 1 1NC127 3 16 81 new l 1-47 3 2 1B344 3 16 72 new l 1-47 3 1 1B2416 2 19 81 new 1B2503 1 16 78 new l 1-47 3 1 1B2573 2 19 81 new 1NC5 2 18 47 new k 3-11 2 0 1NC126 2 18 47 new 1NC16 0 16 75 new k 1D-39 2/3 0 1NC21 1 16 58 new 1NC54 1 16 59 new 1NC57 1 16 61 new 1NC115 1 16 58 new Ab SEQ Mutations #of Name CDR3 (aa) ID NO (+) Length LC Binding NEUT Relatives 1NC2 A V Y D S S L S L G L 725 0 11 47 + 15 1NC3 A T Y D S Q R S I R L 726 2 11 55 + 1 1NC7 A T Y D S Q G S T R L 727 1 11 51 + 1 1NC9 A A Y D S T F S L P V 728 0 11 53 ? + 2 1NC18 ND ND 1 1NC24 A A Y D S S L S L R L 729 0 11 30 + 2 1NC29 ND ND 1 1NC33 A T Y D T D L S L R L 730 1 11 49 + 1 1NC46 A A Y D S A V S L P V 731 0 11 52 ND 1 1NC48 A A Y D S T L S L R L 732 1 11 37 ND 1 1NC52 A A Y D S T F S L P V 733 0 11 54 ND 1 1NC56 A T Y D T G L S L R L 734 1 11 58 ND 1 1NC60 A T Y D S G W S I R L 735 1 11 46 + 3 1NC66 A A Y D S T L S L R L 736 1 11 33 ND 1 1NC70 A A Y D S T L S L R L 737 1 11 40 ND 1 1NC72 A T Y D S Q G S T R L 738 1 11 51 + 2 1NC94 A T Y D S D G S I R L 739 1 11 41 − 5 1NC95 ND ND 1 1NC107 A T Y D T G L S L R L 740 1 11 58 ND 1 1NC108 A A F D S A L S L P L 741 0 11 51 + 1 1NC109 ND ND 1 1NC110 ND ND 1 1NC116 ND ND 1 1NC118 A T Y D T G L S L R L 742 1 11 54 ND 1 1NC122 G T Y D T S L S L R L 743 1 11 57 ND 1 1NC123 A T Y D S H G S I R L 744 2 11 48 − 1 1NC127 A T Y D S D G S I R L 745 1 11 41 ? + 5 1B344 A T Y D S G W S I R L 746 1 11 46 + 1 1B2416 ND ND 1 1B2503 G T Y D S Q G S T R L 882 1 11 49 ND 1 1B2573 ND − 2 1NC5 Q H R S N W P W T 883 2 9 CD4BS + 1 1NC126 ND ND 1 1NC16 Q Q S F A V P Y T 884 0 9 35 ND ND 1 1NC21 ND ND ND 1 1NC54 ND ND ND 1 1NC57 ND ND ND 1 1NC115 ND ND ND 1

TABLE 3c SEQ Ab Name VH D JH (−) CDR3 (aa) ID NO 8ANC13 1-46 3-16 6 4 D G L G E V A P D Y R Y G I D V 885 8ANC22 1-46 3-16 6 3 D G L G E V A P A Y L Y G I D A 747 8ANC26 1-46 3-16 6 3 D G L G E V A P A Y L Y G I D A 748 8ANC37 1-46 3-16 6 3 D G L G E V A P A Y L Y G I D A 749 8ANC41 1-46 3-16 6 3 D G L G E L A P A Y H Y G I D V 750 8ANC50 1-46 3-16 6 3 D G L G E L A P A Y Q Y G I D V 751 8ANC88 1-46 3-16 6 4 D G L G E V A P D Y R Y G I D V 752 8ANC127 1-46 3-16 6 3 D G L G E V A P A Y L Y G I D A 753 8ANC131 1-46 3-16 6 3 D G L G E V A P D Y R Y G I D V 754 8ANC142 1-69 3-3 ND 2 T S T Y D Q W S G L H H D G V M A F S S 755 8ANC46 1-69 3-22/2-15 3 2 S S G N F E F A F E I 756 8ANC191 1-69 3-22/2-15 3 2 S S G N Y D F A Y D I 757 8ANC196 1-69 3-22/2-15 3 2 S S G N Y D F A F D I 758 8ANC14 1-24 6-13/5-5 4 4 A D R F K V A Q D E G L F V I F D Y 759 8ANC34 1-24 6-13/5-5 4 4 A D P F K V A Q D E G L Y V I F D Y 760 8ANC58 1-24 6-13/5-5 4 4 A D P F K V A Q D E G L Y V I F D Y 761 8ANC168 1-24 6-13/5-5 4 4 A D P F K V A Q D E G L F V I F D Y 762 8ANC5 1-69 4-17/3-10 6 8 D R G D T R L L D Y G D Y E D E R Y Y Y G M D V 763 8ANC7 1-69 4-17/3-10 6 8 D R G D T R L L D Y G D Y E D E R Y Y Y G M D V 764 8ANC9 1-69 4-17/3-10 6 8 D R G D T R L L D Y G D Y E D E R Y Y Y G M D V 765 8ANC77 1-69 4-17/3-10 6 8 D R G D T R L L D Y G D Y E D E R Y Y Y G M D V 766 8ANC107 1-69 4-17/3-10 6 8 D R G D T R L L D Y G D Y E D E R Y Y Y G M D V 767 8ANC108 1-69 4-17/3-10 6 8 D R G D T R L L D Y G D Y E D E R Y Y Y G M D V 768 8ANC137 1-69 4-17/3-10 6 8 D R G D T R L L D Y G D Y E D E R Y Y Y G M D V 769 8ANC16 1-69 2-2 3 2 D R S S A I G Y C S S I S C Y K G S F D I 770 8ANC24 1-24 2-2 6 1 G G L Y C S S I S C I M D V 771 8ANC25 1-24 2-2 6 1 G G L Y C S S I S C I M D V 772 8ANC38 3-43 3-16 5 1 N G F D V 773 Mutations Primer Ab Name (+) Length HC Set k/l Vk/l Jk/l (−) 8ANC13 1 16 75 new k 3-11 2/3 1 8ANC22 0 16 85 new 8ANC26 0 16 76 new k 3-11 2/3 1 8ANC37 0 16 82 new k 3-11 2/3 1 8ANC41 1 16 71 new k 3-11 2/3 1 8ANC50 0 16 71 new k 3-11 2/3 1 8ANC88 0 16 73 new k 3-11 2/3 1 8ANC127 0 16 86 new 8ANC131 1 16 75 new k 3-11 2/3 1 8ANC142 2 20 72 new k 1-5 1/5 1 8ANC46 0 11 30 old l 1-40 3 1 8ANC191 0 11 28 old 8ANC196 0 11 25 old 8ANC14 1 18 11 old k 3-11 4 0 8ANC34 0 18 10 new 8ANC58 0 18 18 new 8ANC168 1 18 11 new 8ANC5 3 24 40 old k 1D-33 2 0 8ANC7 3 24 37 new 8ANC9 3 24 35 old 8ANC77 3 24 50 old 8ANC107 3 24 38 old 8ANC108 3 24 37 old 8ANC137 3 24 37 new 8ANC16 1 21 12 old k 3-15 2 0 8ANC24 0 14 12 old k 3-15 1 0 8ANC25 0 14 6 old 8ANC38 0 5 70 new l 2-11 3 0 SEQ ID Mutations #of Ab Name CDR3 (aa) NO (+) Length LC Binding NEUT Relatives 8ANC13 Q E Y S S T P Y N 774 0 9 50 + 1 8ANC22 ND ND 1 8ANC26 Q E Y S S T P Y N 775 0 9 55 CD4BS + 2 8ANC37 Q E Y S S T P Y N 776 0 9 50 CD4BS + 8 8ANC41 Q E Y S S T P Y N 777 0 9 42 + 2 8ANC50 Q E Y S S T P Y N 778 0 9 46 CD4BS + 2 8ANC88 Q E Y S S T P Y N 779 0 9 46 ND 1 8ANC127 ND ND 1 8ANC131 Q E Y S S T P Y N 780 0 9 45 CD4BS + 1 8ANC142 Q Q Y D T Y P 781 0 9 43 ? + 2 G T 8ANC46 Q S Y D R S L R 782 1 11 30 ND ND 1 G S V 8ANC191 ND ND 1 8ANC196 ND ND 1 8ANC14 Q Q R A N W R 783 2 10 9 CD4i + 2 L L T 8ANC34 ND ND 5 8ANC58 ND ND 3 8ANC168 ND ND 1 8ANC5 Q Q Y S N L P Y T 784 0 9 17 CD4i − 2 8ANC7 ND ND 2 8ANC9 ND ND 1 8ANC77 ND ND 3 8ANC107 ND ND 2 8ANC108 ND ND 4 8ANC137 ND ND 1 8ANC16 Q Q Y Y Q W L 785 0 10 13 ND ND 8 S Y T 8ANC24 Q Q Y N H W P 786 0 9 7 CD4i + 1 Q T 8ANC25 ND ND 1 8ANC38 C L K K T S S Y V 787 2 9 41 CORE + 2

TABLE 3d Ab Name VH D JH (−) CDR3 (aa) SEQ ID NO 12A1 1-2 5-12/3- 4/5 4 D E S G D D L K W H L H P 886 10 12A2 1-2 4-17 4/5 3 D G S G D D T S W H L H P 788 12A4 1-2 5-12/3- 4/5 4 D E S G D D L K W H L H P 789 10 12A6 1-2 1-26/3- 4/5 2 D G S G D A T S W H L H P 790 10 12A7 1-2 1-26 4/5 4 D G S G D A R D W H L D P 791 12A9 1-2 3-3 4/5 5 D R R D D D R A W L L D P 792 12A12 1-2 1-26/3- 4/5 4 D G S G D D T S W H L D P 793 10 12A13 1-2 1-26 4/5 4 D G S G D D T S W Y L D P 794 12A20 1-2 1-26 4/5 3 D G S G D A R D W H L H P 795 12A22 1-2 3-16 4/5 4 D G G G D D R T W L L D A 796 12A23 1-2 3-3 4/5 5 D R R D D G L D W L L D P 797 12A27 1-2 1-26/3- 4/5 3 D G S G D D T S W H L H P 798 10 12A46 1-2 3-10 4/5 1 G G G D G R N W H L H P 799 12A55 1-2 1-26 4/5 4 D G S G D D R N W H L D P 800 12A56 1-2 1-26 4/5 4 D E S G Y D L N W H L D S 801 Ab Primer Name (+) Length #Mutations HC Set k/l Vk/l Jk/l (−) 12A1 2 13 60 new k 1D-33 3 0 12A2 2 13 67 new k 1D-33 3 10 12A4 2 13 59 new k 1D-33 3 0 12A6 2 13 61 new k 1D-33 3 1 12A7 1 13 62 new k 1D-33 3 1 12A9 3 13 62 new k 1D-33 3 1 12A12 1 13 60 new k 1D-33 3 1 12A13 0 13 61 new k 1D-33 3 1 12A20 3 13 61 new k 1D-33 3 1 12A22 1 13 61 new k 1D-33 3 1 12A23 2 13 51 new k 1D-33 3 1 12A27 2 13 68 new k 1D-33 3 1 12A46 3 13 62 new k 1D-33 3 1 12A55 1 13 63 new k 1D-33 3 2 12A56 1 13 66 new k 1D-33 3 1 Ab Mutations # of Name CDR3 (aa) SEQ ID NO (+) Length LC Binding NEUT Relatives 12A1 A A F Q W 887 0 5 39 ND 1 12A2 A V L E F 802 0 5 44 + 3 12A4 A V F Q W 803 0 5 36 CD4BS + 3 12A6 A V L E F 804 0 5 39 + 1 12A7 A V L E F 805 0 5 41 ND 2 12A9 Q L F E F 806 0 5 39 ND 1 12A12 A V L E F 807 0 5 41 CD4BS + 1 12A13 A V V E F 808 0 5 41 ND 1 12A20 A A L E F 809 0 5 40 + 1 12A22 S V Y E F 810 0 5 39 + 2 12A23 Q L F E F 811 0 5 39 + 1 12A27 A V L E F 812 0 5 40 ND 1 12A46 A S L E F 813 0 5 43 + 1 12A55 E V Y E F 814 0 5 37 + 1 12A56 E S F Q W 815 0 5 37 ND 1

TABLE 3e Ab SEQ ID Name VH D JH (−) CDR3 (aa) NO 3B191 1-2 6-25/6-13/6-6 2/6 3 Q R S D Y W D F D V 816 3B6 4-39 3-9/3-10 3 2 I P Y H S E S Y Y K V V I G 817 G F D V 3B8 1-69 4-17/3-22 4 3 D H G D P R T G Y Y F D Y 818 3B27 3-64 3-9/1-26/4-17 5 1 G P L L R Y L D S 819 3B41 1-24 3-16 6 4 K A K D Y Y Y E S S D Y S 820 P Y Y Y Y Y M D V 3B46 4-31 3-3/2-8 4/5 0 G S G R W T I G A R I Y F D N 821 3B144 3-30 3-3/3-10/3-16 4/5 2 T P P H Y D V L T G Y P S 822 S V L E F 3B117 1-69 5-5/5-18/5-24 3 2 A T G Y S Y G Y L D A F D I 823 3A869 4-4/4-59 6-19/5-12/1-26 4 2 E K G Q W L T V P P Y Y F 824 D S 3A228 5-51 3-3/2-2 6 1 T R C F G A N C F N F M D V 825 3A461 1-46 2-2 4 1 P E P S S I V A P L Y Y 826 3A18 1-69 3-10/5-24 3 3 D P Q V E V R G N A F D I 827 3A125 1-46 1-20/1-7/3-10 3 2 P Q Y N L G R D P L D V 828 3A255 4-59 3-3/3-9 4 3 A D Y D L L T S S Y H F D S 829 3A233 4-59/4-61 3-3/4-17 4/5 3 L D G E A F R Y Y L D L 830 Ab #Mutations Name (+) Length HC Primer Set k/l Vk/l Jk/l (−) 3B191 1 10 81 new k 1D-33 3 1 3B6 1 18 50 new k 1-9 1/3 0 3B8 2 13 50 new k 3-20 1/5 2 3B27 0 9 18 old k 3-11 1/5 0 3B41 2 22 17 old k 3-20 2 0 3B46 2 15 22 old k 3-20 1/4 0 3B144 1 18 23 old k 3-15 1/5 0 3B117 0 14 22 new l 1-44 1 2 3A869 1 1 33 old k 1D-39 5 0 3A228 1 1 34 old k 4-1 3 0 3A461 0 1 15 old k 3-20 1 0 3A18 1 1 40 old k 1D-39 5 0 3A125 1 1 22 old k 3-20 1 0 3A255 1 1 35 old l 7-43 3 0 3A233 1 1 32 old l 2-14 2/3 0 Ab SEQ ID # of Name CDR3 (aa) NO (+) Length Binding NEUT Relatives 3B191 Q V Y E F 831 0 5 CD4BS + 7 3B6 Q Q L A T 832 0 5 GP41 + 11 3B8 Q Q Y D D A P I T 833 0 9 GP41 − 9 3B27 Q H R T N W P P S I T 834 2 11 CD4i − 3 3B41 Q Q Y G T S S C T 835 0 9 CD4i − 2 3B46 Q Q Y G S S P P T 836 0 9 GP41 ND 2 3B144 Q Q Y N N W P P I T 837 0 10 ND ND 4 3B117 A A W D D T L Y V 838 0 9 ND ND 1 3A869 Q Q S H S P S 839 1 7 CD4BS + 1 3A228 Q Q Y Y I S P 840 0 7 VAR + 4 3A461 Q Q Y G T L H P R T 841 2 10 GP41 − 3 3A18 Q Q T Y T S P I T 842 0 9 GP41 − 2 3A125 Q Q Y G L S P W T 843 0 9 GP41 − 4 3A255 L L L P Y Y G G P W I 844 0 11 GP41 − 2 3A233 S S F T P T N T L V 845 0 10 GP41 − 2

TABLE 3f Ab SEQ ID Name VH D JH (−) CDR3 (aa) NO 1B2434 15341 3-22/5-5 1 4 N E A D Y H D G N G H S L R G M F D Y 846 1B218 1-69 3-3 3 1 G R Q T F R A I W S G P P V V F D I 847 1B331 4-34 3-9/3-3 6 3 R Y F D W S P F R R D T Y G T D V 848 1B2174 4-34 3-9/3-3 6 3 R Y L D W S P I G R D T Y G T D V 849 1B2055 1-69 2-21 2/5 1 G L C R G G N C R L G P S G W L D P 850 1B2133 1-3 4-17/2-21 4 1 V A Y V H V V T T R S L D N 851 1A64 4-59 5-5/5-18 6 2 H E A P R Y S Y A F R R Y Y H Y G L D V 852 1A621 4-59 3-3/3-9 6 1 V I S G R I T I F Y Y N Y I D V 853 1A577 3-48 3-10/3-16 1 3 G T L W F G E S G L R L D H 854 1A732 3-7/3-73 3-22/3-10 6 2 N R R V A M P E A M I L S F Y M D V 855 1A74 4-34 3-3/3-9 4 1 V V P M F S I F G V V K A N Y F D Y 856 1A695 4-59 3-3/3-9 3 2 A G L D Y N F W N G K G R K G A F D V 857 1A479 1-69 3-22 4 1 G F R G S P F S S G S L Y F D S 858 1A182 1-69 4-17/1-26 6 6 A V I T D L H T F G D Y E L E D P S Y 859 Y Y M D V 1A693 3-23 7-27/3-22 4 1 R G R R Q I G D Y 860 1A79 5-51 3-9/3-3 3 4 S Y Y D F S I G D G N D A F D V 861 1A27 3-11 3-6/5-5 5 2 D T T T F T T F G G G P N M G G F D P 862 # Ab Mutations Primer Name (+) Length HC Set k/l Vk/l Jk/l (−) 1B2434 2 19 74 new l 1-47 3 1 1B218 2 18 47 new k 3-11 2 0 1B331 3 17 40 new k 4-1 1/4 0 1B2174 2 17 41 new k 4-1 1/4 0 1B2055 2 18 62 new k 3-15 1 2 1B2133 1 14 22 new k 1D-39 1 0 1A64 5 20 20 old l 1-44 3 2 1A621 1 16 30 old l 1-47 3 1 1A577 1 14 15 old k 1-16 2 0 1A732 2 18 9 old k 3-20 3 0 1A74 1 18 23 old l 1-51 3 1 1A695 3 19 9 old k 1-5 1 1 1A479 1 16 25 old k 3-20 1 0 1A182 1 24 28 old k 1-5 1 0 1A693 3 9 17 old k 1D-39 2 0 1A79 0 16 30 old l 1-47 1 3 1A27 0 19 50 old 1-9 1 0 Ab SEQ # of Name CDR3 (aa) ID NO (+) Length Binding NEUT Relatives 1B2434 A V Y D S S L S L G L 863 0 11 CD4BS + 7 1B218 Q H R S N W P W T 864 2 9 CD4BS + 10 1B331 H Q Y F S T P R T 865 2 9 CORE + 4 1B2174 H Q Y F N T P R T 866 2 9 ND 1 1B2055 Q Q Y E D P P W T 867 0 9 ND ND 3 1B2133 Q Q T Y S N P R M 868 1 9 CD4i − 2 1A64 A S W D D S L S G W V 869 0 11 CD4BS + 24 1A621 A S W D N S L S G P V 870 0 11 CD4BS + 3 1A577 Q Q Y N S F P P T 871 0 9 CD4BS + 8 1A732 Q Q Y G R S P 872 1 7 CD4BS + 1 1A74 G T W D S S L S A V L 873 0 11 CORE + 2 1A695 Q Q Y D S 874 0 5 CORE + 2 1A479 H Q Y A Y S P R T 875 2 9 CORE + 11 1A182 Q Q Y K S Y S G T 876 0 9 CD4i + 3 1A693 Q H S F G S P P W T 877 1 11 CD4i − 1 1A79 A A W D D S F D Y V 878 0 10 V3 + 27 1A27 Q Q L R T 879 1 5 G P 41 − 8

TABLE 4a Patient 3, Clone RU01 3BNC62 3BNC176 3BNC60 3BNC117 3BNC95 3BNC104 MW965.26 <0.09 <0.10 <0.04 <0.09 <0.07 >50 BaL.26 <0.09 <0.10 <0.04 <0.09 <0.07 0.025 DJ263.8 <0.09 <0.10 <0.04 <0.09 <0.07 0.054 6535.3 0.68 0.46 0.54 0.55 1.0 >50 RHPA4259.7 <0.09 <0.10 <0.05 0.041 <0.07 0.0252 TRO.11 <0.09 <0.10 <0.05 0.077 <0.07 3.791 PVO.4 <0.09 <0.10 0.09 <0.09 <0.07 0.348 YU2.DG <0.09 <0.10 <0.05 0.054 <0.07 0.034 3BNC91 3BNC55 3BNC89 3ANC3 3BNC53 3BNC72 MW965.26 <0.08 0.04 >0.05 0.18 0.09 <0.06 BaL.26 >178 >30 >110 >50 >30 >139 DJ263.8 >178 >30 >110 >50 >30 >139 6535.3 1 2.6 1.7 >50 13.6 8.49 RHPA4259.7 <0.08 2.2 12.4 7.66 100.6 >139 TRO.11 3.06 18.4 52.4 10.76 >155 >139 PVO.4 0.44 3.9 2.7 36.77 >155 >139 YU2.DG <0.08 0.9 0.39 35.01 >155 >139 3BNC156 3BNC158 3BNC153 3BNC108 MW965.26 0.08 0.11 0.15 ND BaL.26 >111 >109 >100 20.6 DJ263.8 >111 >109 >100 >55 6535.3 11.1 9.9 28.9 >55 RHPA4259.7 >111 >109 >100 45.91 TRO.11 >111 >109 >100 >55 PVO.4 >111 >109 >100 >55 YU2.DG >111 >109 >100 25.5 3BNC142 3BNC66 3BNC42 3BNC102 MW965.26 0.14 1.24 ND >50 BaL.26 >172 >189 >26 >50 DJ263.8 >172 >189 >26 >50 6535.3 >172 >189 >26 >50 RHPA4259.7 >172 >189 >26 >50 TRO.11 >172 >189 >26 >50 PVO.4 >172 >189 NF >50 YU2.DG >172 >189 >26 >50 Patient 3 Clones RU02-07 3A67 3A383 3BNC8 3ANC44 3A576 3ANC38 MW965.26 0.1 0.5 0.74 25.49 >50 >50 BaL.26 19.2 5.3 >50 27.91 27 >50 DJ263.8 >50 >50 >50 >50 >50 >50 6535.3 >50 ND >50 >50 >50 >50 RHPA4259.7 >50 ND >50 >50 >50 >50 TRO.11 >50 ND >50 >50 >50 >50 PVO.4 >50 ND >50 >50 >50 >50 YU2.DG >50 ND >50 >50 >50 >50 B12 and NIH 45 Clone B12 VRC01 NIH45-46 MW965.26 0.2 <0.08 0.04 BaL.26 0.2 0.1 <0.04 DJ263.8 >50 0.08 <0.04 6535.3 1.4 0.539 0.14 RHPA4259.7 0.1 0.06 0.034 TRO.11 >50 0.2 1.9 PVO.4 >50 0.2 0.17 YU2.DG 2.2 0.12 <0.05

TABLE 4b Patient 1, Clone RU08 1B2640 1B2530 1B2364 1NC2 1NC9 1B2490 MW965.26 41.76 0.762 1.85 >50 >50 >50 BaL.26 0.08 >50 >25 0.11 1.37 0.058 DJ263.8 >50 2.71 3.75 >50 >50 >50 6535.3 >50 >50 >25 >50 >50 >50 RHPA4259.7 0.04 3.6 2.18 0.59 0.09 0.414 TRO.11 0.23 0.516 0.27 0.17 0.2 1.06 PVO.4 1.05 0.275 0.161 0.37 0.34 2.97 YU2.DG 0.2 0.209 2.46 0.12 0.13 0.125 1B2351 1B344 1NC24 1NC3 1NC7 1NC33 MW965.26 >50 >50 >50 >25 >50 >50 BaL.26 >50 >50 >50 >25 >50 >50 DJ263.8 8.46 12.62 >50 >25 >50 >50 6535.3 >50 >50 >50 >25 >50 22.04 RHPA4259.7 36.48 29.98 >50 >25 34.27 >50 TRO.11 0.331 0.27 0.2 3.37 16.57 >50 PVO.4 0.25 0.27 0.19 6.68 1.39 1.84 YU2.DG 0.058 0.25 0.16 18.26 >50 >50 1NC108 1B2644 1B2339 1NC123 MW965.26 >50 >25 >25 >50 BaL.26 >50 >25 >25 >50 DJ263.8 >50 >25 >25 >50 6535.3 >50 >25 >25 >50 RHPA4259.7 >50 >25 >25 >50 TRO.11 19.37 >25 >25 >50 PVO.4 3.13 >25 >25 >50 YU2.DG >50 >25 >25 >50 Patient 1, Clone RU09 1B218 MW965.26 >119 BaL.26 1.1 DJ263.8 >119 6535.3 3.6 RHPA4259.7 >100 TRO.11 >100 PVO.4 >100 YU2.DG >100

TABLE 4c Patient 8, Clone RU10 8ANC192 8ANC134 8ANC13 8ANC131 8ANC182 8ANC50 8ANC45 MW965.26 >73 >50 >50 >50 >115 >50 >50 BaL.26 0.08 0.02 0.04 0.06 0.08 0.17 0.296 DJ263.8 <0.03 0.003 0.008 0.004 <0.05 0.04 0.041 6535.3 0.34 0.06 0.27 0.2 0.89 2.27 0.813 RHPA4259.7 >50 >50 >50 >50 >100 >50 >50 TRO.11 >100 >50 >50 >50 >100 >50 >50 PVO.4 0.89 0.46 0.63 0.81 1.2 3.89 4.259 YU2.DG 0.09 0.15 0.21 0.18 0.22 0.42 0.499 Patient 8, Clones RU11-15 8ANC57 8ANC195 8ANC24 8ANC14 8ACN5 MW965.26 24.1 >50 0.29 2.01 >50 BaL.26 4.35 >50 47.53 >50 >50 DJ263.8 30.19 >50 >50 >50 >50 6535.3 >103 0.2 >50 >50 >50 RHPA4259.7 1.65 0.34 >50 >50 >50 TRO.11 32.07 0.18 >50 >50 >50 PVO.4 101.15 0.52 >50 >50 >50 YU2.DG 27.52 0.79 >50 >50 >50

TABLE 4d Patient 12, Clone RU16 12A12 12A21 12A4 12A37 12A22 12A16 MW965.26 0.042 0.075 0.098 0.056 0.06 0.167 BaL.26 0.017 <0.001 <0.001 0.005 0.04 0.042 DJ263.8 0.002 0.035 0.017 0.013 0.08 0.012 6535.3 21.97 >50 >50 >50 >25 15.44 RHPA4259.7 0.086 0.038 0.041 0.042 0.04 0.207 TRO.11 0.288 0.164 0.257 0.827 0.56 0.751 PVO.4 0.928 0.584 0.819 0.516 0.45 2.44 YU2.DG 0.084 0.015 0.018 0.019 0.11 0.234 12A20 12A6 12A23 12A46 12A55 MW965.26 0.192 0.112 5.1 >50 0.58 BaL.26 0.035 0.072 0.57 0.013 2.87 DJ263.8 0.05 0.004 0.63 5.79 >50 6535.3 48.73 >24 14.73 48.85 >50 RHPA4259.7 0.109 0.227 0.496 >50 >50 TRO.11 0.689 1.52 2.88 >50 21.45 PVO.4 3.04 3.32 2.24 2.18 0.99 YU2.DG 0.142 0.222 0.053 0.49 0.1 B12 and NIH45 Clone B12 VRC01 NIH45-46 MW965.26 0.2 <0.08 0.04 BaL.26 0.2 0.1 <0.04 DJ263.8 >50 0.08 <0.04 6535.3 1.4 0.539 0.14 RHPA4259.7 0.1 0.06 <0.05 TRO.11 >50 0.2 1.9 PVO.4 >50 0.2 0.17 YU2.DG 2.2 0.12 <0.05

TABLE 4e Patient 3, clone RU01 3BNC62 3BNC176 3BNC60 3BNC117 3BNC95 3BNC104 MW965.26 <0.09 <0.10 0.09 <0.09 <0.07 >50 BaL.26 <0.09 <0.10 <0.04 <0.09 <0.07 0.09 DJ263.8 0.1 <0.10 0.1 0.1 0.1 0.187 6535.3 2.24 1.7 1.77 2.44 4.5 >50 RHPA4259.7 <0.09 <0.10 0.07 0.137 <0.07 0.06 TRO.11 <0.09 <0.10 0.12 0.077 <0.07 30.847 PVO.4 0.23 0.16 0.27 0.19 0.23 0.901 YU2.DG <0.09 <0.10 0.07 0.054 <0.07 0.097 3BNC91 3BNC55 3BNC89 3ANC3 3BNC53 3BNC72 3BNC156 MW965.26 <0.08 0.15 0.16 0.64 0.61 0.37 0.47 BaL.26 >178 >30 >110 >50 >30 >139 >111 DJ263.8 >178 >30 >110 >50 >30 >139 >111 6535.3 6.7 5.53 5.92 >50 73.38 133.665 69.66 RHPA4259.7 0.52 8.03 >110 >50 >155 >139 >111 TRO.11 32.31 41.67 >110 >50 >155 >139 >111 PVO.4 2.65 6.5 10.18 >50 >155 >139 >111 YU2.DG <0.08 1.07 1.49 >50 >155 >139 >111 3BNC158 3BNC153 3BNC108 3BNC142 3BNC66 3BNC42 3BNC102 MW965.26 0.6 0.63 ND 0.8 29.98 ND >50 BaL.26 >109 >100 >55 >172 >189 >26 >50 DJ263.8 >109 >100 >55 >172 >189 >26 >50 6535.3 97.75 >100 >55 >172 >189 >26 >50 RHPA4259.7 >109 >100 >55 >172 >189 >26 >50 TRO.11 >109 >100 >55 >172 >189 >26 >50 PVO.4 >109 >100 >55 >172 >189 ND >50 YU2.DG >109 >100 >55 >172 >189 >26 >50 Patient 3, Clones RU02-07 3A67 3A383 3BNC8 3ANC44 3A576 3ANC38 MW965.26 16 >25 0.74 >50 >50 >50 BaL.26 >50 >25 >50 >50 >50 >50 DJ263.8 >50 >25 >50 >50 >50 >50 6535.3 >50 ND >50 >50 >50 >50 RHPA4259.7 >50 ND >50 >50 >50 >50 TRO.11 >50 ND >50 >50 >50 >50 PVO.4 >50 ND >50 >50 >50 >50 YU2.DG >50 ND >50 >50 >50 >50 B12 and NIH 45 Clone B12 VRC01 45-46 MW965.26 ND <0.08 0.21 BaL.26 ND 0.1 0.06 DJ263.8 ND 0.553 0.06 6535.3 ND 2.7 0.28 RHPA4259.7 0.39 0.185 0.146 TRO.11 >50 0.832 9.56 PVO.4 >50 1.2 0.47 YU2.DG 7.8 0.372 0.08

TABLE 4f Patient 1, Clone RU08 1B2640 1B2530 1B2364 1NC2 1NC9 1B2490 1B2351 MW965.26 >50 >50 >25 >50 >50 >50 >50 BaL.26 0.32 >50 >25 0.51 19.92 0.3 >50 DJ263.8 >50 >50 >25 >50 >50 >50 >50 6535.3 >50 >50 >25 >50 >50 >50 >50 RHPA4259.7 0.25 >50 >25 4.33 0.4 1.97 >50 TRO.11 1.62 2.46 1.77 0.55 0.65 3.58 1.13 PVO.4 2.97 1.25 0.65 1.08 1.32 10.57 0.88 YU2.DG 0.7 7.74 >25 0.39 0.56 0.59 0.48 1B344 1NC24 1NC3 1NC7 1NC33 1NC108 1B2644 MW965.26 >50 >50 >25 >50 >50 >50 >25 BaL.26 >50 >50 >25 >50 >50 >50 >25 DJ263.8 >50 >50 >25 >50 >50 >50 >25 6535.3 >50 >50 >25 >50 >50 >50 >25 RHPA4259.7 >50 >50 >25 >50 >50 >50 >25 TRO.11 0.89 0.66 >25 >50 >50 >50 >25 PVO.4 0.94 0.6 >25 7.17 10.12 25.08 >25 YU2.DG 1.29 0.55 >25 >50 >50 >50 >25 Patient 1, Clone RU08 Patient 1, Clone RU09 1B2339 1NC123 1B218 MW965.26 >25 >50 >119 BaL.26 >25 >50 5.61 DJ263.8 >25 >50 >119 6535.3 >25 >50 35.12 RHPA4259.7 >25 >50 >100 TRO.11 >25 >50 >100 PVO.4 >25 >50 >100 YU2.DG >25 >50 >100

TABLE 4g Patient 8, Clone RU 10 8ANC192 8ANC134 8ANC13 8ANC131 8ANC182 8ANC50 8ANC45 TRO.11 >73 >50 >50 >50 >115 >50 >50 BaL.26 0.43 0.11 0.18 0.31 0.73 0.77 7.45 DJ263.8 0.1 0.044 0.069 0.046 0.11 0.15 0.166 6535.3 1.43 2 2.3 1.9 3.93 13.65 10.473 RHPA4259.7 >100 >50 >50 >50 >100 >50 >50 TRO.11 >100 >50 >50 >50 >100 >50 >50 PVO.4 3.94 2.5 3.7 4.9 4.43 14.99 17.315 YU2.DG 0.51 0.616 1.07 0.92 1.46 1.59 2.942 Patient 8, Clones RU11-15 8AN57 8AN195 8AN24 8AN14 8AN5 TRO.11 >103 >50 0.76 6.64 >50 BaL.26 24.76 >50 >50 >50 >50 DJ263.8 >103 >50 >50 >50 >50 6535.3 >103 0.91 >50 >50 >50 RHPA4259.7 14.44 1.56 >50 >50 >50 TRO.11 >103 0.89 >50 >50 >50 PVO.4 >103 1.87 >50 >50 >50 YU2.DG 91.49 2.77 >50 >50 >50

TABLE 4h Patient 12, Clone RU16 12A12 12A21 12A4 12A37 12A22 12A16 MW965.26 0.2 0.85 1.24 0.3 0.21 0.58 BaL.26 0.08 0.004 0.007 0.03 0.14 0.25 DJ263.8 0.31 0.42 1.06 0.57 1.86 0.12 6535.3 >50 >50 >50 >50 >25 >42 RHPA4259.7 0.4 0.13 0.19 0.19 0.13 0.93 TRO.11 0.98 0.57 1.12 3.81 1.94 2.57 PVO.4 3.15 2.09 2.95 1.8 1.49 8.72 YU2.DG 0.31 0.06 0.1 0.07 0.36 1.13 12A20 12A6 12A23 12A46 12A55 MW965.26 2.2 0.52 >50 >50 4.49 BaL.26 0.23 0.47 3.47 0.08 >50 DJ263.8 ND 0.08 30.81 >50 >50 6535.3 ND >24 >50 >50 >50 RHPA4259.7 0.49 1.02 1.69 >50 >50 TRO.11 2.41 5.15 10.11 >50 >50 PVO.4 11.2 17.34 7.81 797 4.3 YU2.DG 0.67 1.2 0.19 0.25 0.29 B12 and NIH45 Clone B12 VRC01 NIH45-46 MW965.26 0.2 <0.08 0.04 BaL.26 0.2 0.1 <0.04 DJ263.8 >50 0.08 <0.04 6535.3 1.4 0.539 0.14 RHPA4259.7 0.1 0.06 <0.05 TRO.11 >50 0.2 1.9 PVO.4 >50 0.2 0.17 YU2.DG 2.2 0.12 <0.05

TABLE 5a In vitro Tzm-bl neutralization assay, extended panel IC50 values B12 VRC01 NIH45-46 3BNC60 3BNC62 3BNC117 3BNC55 Q842.d12 >50 0.03 0.008 0.01 <0.01 <0.01 0.011 3415.v1.c1 2.5 0.06 0.017 0.1 0.17 0.17 0.11 3365.v2.c20 >50 0.03 0.029 0.02 0.03 0.03 0.221 H086.8* >50 >50 >30 >15 >15 >15 >30 ZM53M.PB12 >50 1.3 0.187 0.22 0.3 0.21 12.549 Du172.17* 0.3 >50 >30 3.81 1.72 1.19 3.518 ZM109F.PB4 >50 0.128 0.059 0.22 0.14 0.14 0.083 3016.v5.c45 1.1 0.16 >30 1.4 0.42 1.38 >30 231965.c1 0.07 0.34 0.021 0.07 0.05 0.05 0.505 X1254_c3 >50 0.07 0.027 0.09 0.08 0.08 0.138 250-4* >50 >50 >30 >15 >15 >15 0.236 251-18 >50 2.5 1.445 0.35 0.32 0.26 >30 278-50* >50 >50 >30 >15 >15 >15 >30 620345.c1* >50 >50 >30 >15 >15 >15 >30 R1166.c1 >50 1.7 0.445 0.14 0.32 0.17 0.298 1NC9 1B2530 8ANC131 8ANC134 8ANC195 12A12 12A21 Q842.d12 0.02 0.249 0.053 0.061 >30 0.014 0.015 3415.v1.c1 0.266 0.065 0.299 0.323 2.404 0.121 0.82 3365.v2.c20 0.329 4.357 >30 >30 >30 0.068 0.045 H086.8* >30 >30 >50 >50 0.095 >30 >30 ZM53M.PB12 0.705 0.912 >30 >30 9.626 0.593 0.42 Du172.17* >30 >30 >30 >30 10.797 0.196 0.126 ZM109F.PB4 0.023 >30 >30 >30 >30 0.148 2.104 3016.v5.c45 >30 >30 >30 >30 0.195 1.163 0.097 231965.c1 0.393 0.168 6.346 >30 0.514 2.217 >30 X1254_c3 >30 >30 >30 >30 1.524 1.032 26.793 250-4* >30 >30 >50 >50 >50 >30 >30 251-18 1.234 9.847 0.968 1.56 0.284 2.622 1.713 278-50* >30 >30 >50 >50 >50 >30 >30 620345.c1* >30 >30 >50 >50 >50 >30 >30 R1166.c1 0.651 0.119 >30 >30 0.986 0.342 0.292

TABLE 5b In vitro Tzm-bl neutralization assay, extended panel IC80 values B12 VRC01 45-46 3BNC60 3BNC62 3BNC117 3BNC55 Q842.d12 >50 0.096 0.026 0.03 0.03 0.01 0.062 3415.v1.c1 14.1 0.15 0.069 0.37 0.4 0.47 0.388 3365.v2.c20 >50 0.17 0.114 0.08 0.09 0.1 2.341 H086.8* >50 >50 >30 >15 >15 >15 >30 ZM53M.PB12 >50 4 0.652 0.76 1.1 0.85 >30 Du172.17* 2.6 >50 >30 >15 12.18 8.9 >30 ZM109F.PB4 >50 0.754 0.22 1.23 0.78 0.88 0.396 3016.v5.c45 4 0.42 >30 7.38 2.35 >15 >30 231965.c1 0.16 1.2 0.1 0.25 0.22 0.22 2.78 X1254_c3 >50 0.19 0.078 0.29 0.27 0.27 0.571 250-4* >50 >50 >30 >15 >15 >15 1.922 251-18 >50 11.2 5.255 0.96 1 0.82 >30 278-50* >50 >50 >30 >15 >15 >15 >30 620345.c1* >50 >50 >30 >15 >15 >15 >30 R1166.c1 >50 4.6 1.679 0.51 0.89 0.64 2.351 1NC9 1B2530 8ANC131 8ANC134 8ANC195 12A12 12A21 Q842.d12 0.133 2.191 0.179 0.205 >30 0.06 0.066 3415.v1.c1 1.002 0.35 1.555 2.643 17.743 0.418 0.296 3365.v2.c20 2.163 >30 >30 >30 >30 0.192 0.166 H086.8* >30 >30 >50 >50 5.328 >30 >30 ZM53M.PB12 2.771 4.022 >30 >30 >30 2.069 1.458 Du172.17* >30 >30 >30 >30 >30 0.992 0.637 ZM109F.PB4 0.146 >30 >30 >30 >30 0.698 13.686 3016.v5.c45 >30 >30 >30 >30 0.872 11.864 0.358 231965.c1 2.276 0.963 >30 >30 2.355 15.102 >30 X1254_c3 >30 >30 >30 >30 6.949 5.777 >30 250-4* >30 >30 >50 >50 >50 >30 >30 251-18 6.291 >30 5.55 6.281 1.511 9.39 6.063 278-50* >30 >30 >50 >50 >50 >30 >30 620345.c1* >30 >30 >50 >50 >50 >30 >30 R1166.c1 2.669 0.684 >30 >30 4.83 1.85 2.137

TABLE 6 Affinity of IgG Antibodies to YU-2 gp140 and 2CC-core Ligands Measured by Surface Plasmon Resonance gp140 2CC-Core k_(a) (M⁻¹s⁻¹) k_(d) (s⁻¹) K_(D) (M) ka (M⁻¹s⁻¹) k_(d) (s⁻¹) K_(D) (M) 12A12 4.59E+04 1.44E−05 3.15E−10 6.33E+04 1.70E−06 2.69E−11 12A21 9.18E+04 3.44E−07 3.75E12 1.82E+05 3.30E−04 1.81E−09 12AGL / / / / / / 3BNC60 2.73E+04 1.86E−04 6.81E−09 3.02E+04 1.64E−03 5.45E−08 3BNC117 3.04E+04 1.99E−04 6.54E−09 1.49E−03 4.05E+04 3.68E−08 3BNC55 1.31E+04 7.55E−04 5.78E−08 8.15E−04 3.16E+04 2.57E−08 3BNC66 1.60E+04 1.41E−03 8.81E−08 3.96E+04 1.33E−03 3.36E−08 3BNC156 1.13E+04 1.98E−03 1.75E−07 1.88E+04 1.53E−03 8.12E−08 3BNC108 / / / / / / 3BNC60GL / / / / / / 8ANC131 6.59E+04 1.09E−03 1.65E−08 4.88E+04 3.23E−03 6.61E−08 8ANC134 1.55E+04 1.74E−03 1.13E−07 2.08E+04 9.57E−04 4.61E−08 8AGL / / / / / / 8ANC195 4.88E+04 1.67E−03 3.43E−08 2.41E+04 1.32E−03 5.47E−08 1NC9 4.83E+04 5.81E−04 1.20E−08 5.11E+04 2.36E−04 4.61E−09 1B2530 4.74E+04 1.62E−03 3.42E−08 6.83E+04 4.02E−04 5.90E−09 1GL / / / / / / 4546 4.26E+04 2.87E−04 6.75E−09 1.12E+05 4.94E−04 4.40E−09 VRC01 1.83E+04 8.08E−06 4.41E−10 2.84E+04 3.25E−05 1.15E−09

TABLE 7a Replacement/Silent mutation ratios for heavy chain sequences of 10 selected antibodies Consensus Non Consensus All Nucleotides Nucleotides Nucleotides 3BNC117HC 1.8 1.0 3.5 3BNC60HC 2.0 1.1 4.4 12A12HC 2.8 1.7 6.3 12A21HC 2.6 1.5 4.8 NIH4546HC 1.7 0.9 5.5 VRCO1HC 2.2 1.1 22.0 8ANC131HC 2.7 1.3 8.0 8ANC134HC 2.2 1.5 3.7 1B2530HC 2.0 0.9 11.0 1NC9HC 1.9 0.7 12.0

TABLE 7b Replacement/Silent mutation ratios for light chain sequences of 10 selected antibodies Consensus Non Consensus All Nucleotides Nucleotides Nucleotides 3BNC117KC 1.7 0.8 2.8 3BNC60KC 1.7 0.7 4.0 12A12KC 1.7 0.6 4.0 12A21KC 2.5 1.4 4.3 NIH4546KC 1.7 0.9 3.0 VRCO1KC 1.8 0.8 4.0 8ANC131KC 1.5 0.5 4.2 8ANC134KC 1.5 0.5 4.2 1B2530LC 1.9 2.0 1.8 1NC9LC 1.2 0.9 1.8

TABLE 8 Crystallization data collection and refinement statistics Crystal 3BN60 Fab Data collection* Wavelength (Å) 0.9537 Space group P21 Unit Cell dimensions a (Å) 63.6 b (Å) 155.7 c (Å) 74.8 α, β, γ (Y)     90.0, 110.4, 90.0 Resolution, (Å) 39.172.65 R_(mrgd)-F (%)^(§) 8.3 (55.5) R_(meas) (%)^(§) 7.7 (53.4) I/σI 15.7 (2.5) Completeness (%) 96.0 (68.1) Multiplicity 5.0 (3.6) Reflections 192709 Unique reflections 38111 Refinement Resolution (Å) 39.172.65 No. reflections 37086 R_(work)/R_(free) (%)^(†) 20.7/25.7 RMSD Bond lengths (Å) 0.01 RMSD Bond angles (Y) 1.3 Average B-factor Å² 64.9 Ramachandran analysis Favored (%) 91.9 Allowed (%) 7.6 Outlier (%) 0.5 

What is claimed is:
 1. A polynucleotide comprising a nucleic acid sequence encoding an anti-HIV antibody or an HIV gp120-derived antigen-binding fragment thereof comprising the CDR1, CDR2, and CDR3 regions of the sequence of SEQ ID NO: 387 and the CDR1, CDR2, and CDR3 regions of the sequence of SEQ ID NO:
 558. 2. The polynucleotide of claim 1, wherein the anti-HIV antibody or an HIV gp120-derived antigen-binding fragment thereof comprises the sequences of SEQ ID NO: 387 and SEQ ID NO:
 558. 3. The polynucleotide of claim 1, wherein the nucleic acid sequence comprises SEQ ID NOs: 993 and
 1013. 4. The polynucleotide of claim 1, wherein the polynucleotide is a DNA, cDNA or RNA molecule.
 5. A vector comprising the polynucleotide of claim
 1. 6. The vector of claim 5, wherein the vector comprises the polynucleotide of claim
 2. 7. The vector of claim 5, wherein the vector comprises the polynucleotide of claim
 3. 8. The vector of claim 5 is a lentiviral vector.
 9. A cell comprising the vector of claim
 5. 10. The cell of claim 9, wherein the cell comprises the vector of claim
 6. 11. The cell of claim 9, wherein the cell comprises the vector of claim
 7. 12. A pharmaceutical composition comprising the polynucleotide of claim 1 and optionally a pharmaceutically acceptable carrier.
 13. The pharmaceutical composition of claim 12, wherein the pharmaceutical composition comprises the polynucleotide of claim
 2. 14. The pharmaceutical composition of claim 12, wherein the pharmaceutical composition comprises the polynucleotide of claim
 3. 15. A method for treating HIV infection or an HIV-related disease comprising: (a) identifying a patient in need of such treatment, and (b) administering to the patient a therapeutically effective amount of the polynucleotide of claim
 1. 16. The method of claim 15, wherein the method comprises administering to the patient a therapeutically effective amount of the polynucleotide of claim
 2. 17. The method of claim 15, wherein the method comprises administering to the patient a therapeutically effective amount of the polynucleotide of claim
 3. 